Human (GRCh38.p14)
Description

solute carrier family 22 member 31 [Source:HGNC Symbol;Acc:HGNC:27091]

Location
About this transcript

This transcript has 9 exons, is annotated with 25 domains and features, is associated with 3035 variant alleles and maps to 327 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000682282.1SLC22A31-2071615446aaENSP00000508250.1
 
Protein coding
CCDS92209A0A804HL90 NM_001384763.1MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1
ENST00000562855.7SLC22A31-2011945338aaENSP00000474621.2
 
Protein coding
CCDS73927A6NKX4 -GENCODE basicTSL:5
ENST00000614943.4SLC22A31-2061860338aaENSP00000481421.1
 
Protein coding
CCDS73927A0A087WY01 -GENCODE basicTSL:5
ENST00000603735.1SLC22A31-205791No protein-
 
Retained intron
--TSL:3
ENST00000563595.6SLC22A31-203780No protein-
 
Retained intron
--TSL:3
ENST00000562916.1SLC22A31-202692No protein-
 
Retained intron
--TSL:5
ENST00000568161.2SLC22A31-204651No protein-
 
Retained intron
--TSL:3
Statistics

Exons: 9, Coding exons: 9, Transcript length: 1,615 bps, Translation length: 446 residues

MANE

This MANE Select transcript contains ENSP00000508250 and matches to NM_001384763.1 and NP_001371692.1

CCDS

This transcript is a member of the Human CCDS set: CCDS92209

Version

ENST00000682282.1

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.