Human (GRCh38.p14)
Description

ATP binding cassette subfamily B member 1 [Source:HGNC Symbol;Acc:HGNC:40]

Gene Synonyms

ABC20, CD243, CLCS, GP170, MDR1, P-170, P-GP, PGY1

Location

Chromosome 7: 87,503,017-87,713,323 reverse strand.

GRCh38:CM000669.2

About this gene

This gene has 11 transcripts (splice variants), 161 orthologues, 10 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000622132.5ABCB1-21152051280aaENSP00000478255.1
 
Protein coding
CCDS5608P08183-1 NM_001348946.2MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000265724.8ABCB1-20147201280aaENSP00000265724.3
 
Protein coding
CCDS5608P08183-1 -GENCODE basicAPPRIS P1TSL:1
ENST00000543898.5ABCB1-21045241216aaENSP00000444095.1
 
Protein coding
P08183-2 -GENCODE basicTSL:5
ENST00000416177.1ABCB1-20246148aaENSP00000399419.1
 
Protein coding
E7EWT8 -TSL:5CDS 3' incomplete
ENST00000488737.6ABCB1-2071864No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000496821.5ABCB1-209913No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000475929.5ABCB1-203787No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000476862.1ABCB1-204582No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000483831.1ABCB1-206642No protein-
 
Retained intron
--TSL:3
ENST00000482527.1ABCB1-205555No protein-
 
Retained intron
--TSL:4
ENST00000491360.1ABCB1-208539No protein-
 
Retained intron
--TSL:2