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Human (GRCh38.p14)
Description

solute carrier family 22 member 12 [Source:HGNC Symbol;Acc:HGNC:17989]

Gene Synonyms

HURAT1, OAT4L, RST, UAT, URAT1

Location
About this transcript

This transcript has 10 exons, is annotated with 38 domains and features, is associated with 7644 variant alleles and maps to 391 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000377574.6SLC22A12-2042792553aaENSP00000366797.1
 
Protein coding
CCDS8075Q96S37-1 NM_144585.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000377572.5SLC22A12-2032887445aaENSP00000366795.1
 
Protein coding
CCDS60836Q96S37-2 -GENCODE PrimaryGENCODE BasicTSL:1
ENST00000377567.6SLC22A12-2022599445aaENSP00000366790.2
 
Protein coding
CCDS60836Q96S37-2 -GENCODE PrimaryGENCODE BasicTSL:5
ENST00000473690.5SLC22A12-2052522332aaENSP00000438437.1
 
Protein coding
Q96S37-3 -GENCODE PrimaryGENCODE BasicTSL:2
ENST00000336464.7SLC22A12-2011854519aaENSP00000336836.7
 
Protein coding
CCDS60835Q96S37-4 -GENCODE PrimaryGENCODE BasicTSL:1
Statistics

Exons: 10, Coding exons: 10, Transcript length: 1,854 bps, Translation length: 519 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q96S37

CCDS

This transcript is a member of the Human CCDS set: CCDS60835

Transcript Support Level (TSL)

TSL:1

Version

ENST00000336464.7

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.

GENCODE primary gene

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