Human (GRCh38.p14)
Description

ATP binding cassette subfamily C member 1 [Source:HGNC Symbol;Acc:HGNC:51]

Gene Synonyms

GS-X, MRP, MRP1

Location

Chromosome 16: 15,949,138-16,143,257 forward strand.

GRCh38:CM000678.2

View alleles of this gene on alternative sequences

About this gene

This gene has 11 transcripts (splice variants), 1 gene allele, 201 orthologues, 11 paralogues and is associated with 2 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000399410.8ABCC1-20265041531aaENSP00000382342.3
 
Protein coding
CCDS42122P33527-1 NM_004996.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000399408.7ABCC1-20165941541aaENSP00000382340.4
 
Protein coding
P33527-9 -GENCODE basicTSL:5
ENST00000572882.3ABCC1-20363871472aaENSP00000461615.2
 
Protein coding
CCDS45427P33527-2 -TSL:1
ENST00000677164.1ABCC1-20962761374aaENSP00000502873.1
 
Protein coding
A0A7I2V2E0 -GENCODE basic
ENST00000678422.1ABCC1-2106445866aaENSP00000503954.1
 
Nonsense mediated decay
A0A7I2V4C6 --
ENST00000676806.1ABCC1-2083077No protein-
 
Protein coding CDS not defined
---
ENST00000679043.1ABCC1-2111770No protein-
 
Protein coding CDS not defined
---
ENST00000576557.1ABCC1-207542No protein-
 
Protein coding CDS not defined
--TSL:4
ENST00000574224.2ABCC1-2042616No protein-
 
Retained intron
--TSL:1
ENST00000575422.5ABCC1-2061198No protein-
 
Retained intron
--TSL:5
ENST00000574761.1ABCC1-205996No protein-
 
Retained intron
--TSL:2