Human (GRCh38.p14)
Description

transporter 1, ATP binding cassette subfamily B member [Source:HGNC Symbol;Acc:HGNC:43]

Gene Synonyms

ABCB2, D6S114E, PSF1, RING4

Location

Chromosome 6: 32,845,209-32,853,816 reverse strand.

GRCh38:CM000668.2

View alleles of this gene on alternative sequences

About this gene

This gene has 11 transcripts (splice variants), 1 gene allele, 217 orthologues, 10 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000354258.5TAP1-2012685748aaENSP00000346206.5
 
Protein coding
CCDS4758Q03518-1 NM_000593.6MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000698423.1TAP1-2102793829aaENSP00000513711.1
 
Protein coding
A0A8V8TM76 -GENCODE basic
ENST00000698424.1TAP1-2112515705aaENSP00000513712.1
 
Protein coding
A0A8V8TNH0 -GENCODE basic
ENST00000698422.1TAP1-2092496685aaENSP00000513710.1
 
Protein coding
A0A8V8TN61 -GENCODE basic
ENST00000643049.2TAP1-2041319263aaENSP00000494148.2
 
Protein coding
A0A2R8Y4Y0 -GENCODE basic
ENST00000698420.1TAP1-2072531238aaENSP00000513708.1
 
Nonsense mediated decay
A0A8V8TLN3 --
ENST00000698421.1TAP1-2082474299aaENSP00000513709.1
 
Nonsense mediated decay
A0A8V8TLQ7 --
ENST00000645078.1TAP1-2062170No protein-
 
Protein coding CDS not defined
---
ENST00000643923.1TAP1-2051992No protein-
 
Protein coding CDS not defined
---
ENST00000486332.1TAP1-2022542No protein-
 
Retained intron
--TSL:2
ENST00000487296.1TAP1-2031031No protein-
 
Retained intron
--TSL:5