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Human (GRCh38.p14)
Description

solute carrier family 14 member 2 [Source:HGNC Symbol;Acc:HGNC:10919]

Gene Synonyms

HUT2, UT2

Location
About this transcript

This transcript has 20 exons, is annotated with 76 domains and features, is associated with 30145 variant alleles and maps to 593 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000255226.11SLC14A2-2014073920aaENSP00000255226.5
 
Protein coding
CCDS11924Q15849-1 NM_007163.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1TSL:1
ENST00000586448.5SLC14A2-2033540920aaENSP00000465953.1
 
Protein coding
CCDS11924Q15849-1 -GENCODE PrimaryGENCODE BasicAPPRIS P1TSL:2
ENST00000323329.3SLC14A2-2021729235aaENSP00000320689.3
 
Nonsense mediated decay
E7EPU1 -TSL:2
Statistics

Exons: 20, Coding exons: 19, Transcript length: 4,073 bps, Translation length: 920 residues

MANE

This MANE Select transcript contains ENSP00000255226 and matches to NM_007163.4 and NP_009094.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q15849

CCDS

This transcript is a member of the Human CCDS set: CCDS11924

Transcript Support Level (TSL)

TSL:1

Version

ENST00000255226.11

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.