Human (GRCh38.p14)
Description

solute carrier family 22 member 1 [Source:HGNC Symbol;Acc:HGNC:10963]

Gene Synonyms

OCT1

About this transcript

This transcript has 3 exons, is annotated with 5 domains and features, is associated with 2029 variant alleles and maps to 75 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000366963.9SLC22A1-2021922554aaENSP00000355930.4
 
Protein coding
CCDS5274O15245-1 NM_003057.3MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000324965.8SLC22A1-2011521506aaENSP00000318103.4
 
Protein coding
CCDS5275O15245-2 -GENCODE basicTSL:5
ENST00000457470.6SLC22A1-2031452483aaENSP00000409557.2
 
Protein coding
O15245-3 -GENCODE basicTSL:5
ENST00000540443.1SLC22A1-20765348aaENSP00000440105.1
 
Protein coding
F5GY86 -TSL:3CDS 3' incomplete
ENST00000539263.5SLC22A1-2061598140aaENSP00000443245.1
 
Nonsense mediated decay
F5H5P3 -TSL:5
ENST00000460902.2SLC22A1-2041484353aaENSP00000439274.1
 
Nonsense mediated decay
O15245-4 -TSL:5
ENST00000478607.1SLC22A1-205324No protein-
 
Retained intron
--TSL:2

Protein domains for ENSP00000440105.1