Human (GRCh38.p14)
Description

solute carrier family 13 member 2 [Source:HGNC Symbol;Acc:HGNC:10917]

Gene Synonyms

NADC-1

Location
About this transcript

This transcript has 12 exons, is annotated with 21 domains and features, is associated with 10915 variant alleles and maps to 627 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000314669.10SLC13A2-2012360592aaENSP00000316202.6
 
Protein coding
CCDS11231Q13183-1 NM_003984.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000444914.7SLC13A2-2022855641aaENSP00000392411.3
 
Protein coding
CCDS54098Q13183-3 -GENCODE basicTSL:2
ENST00000579281.5SLC13A2-2062320548aaENSP00000463421.2
 
Protein coding
CCDS92282J3QL78 -GENCODE basicTSL:2
ENST00000459818.2SLC13A2-2032466100aaENSP00000464074.2
 
Nonsense mediated decay
J3QR70 -TSL:2
ENST00000577903.5SLC13A2-2052217No protein-
 
Retained intron
--TSL:2
ENST00000541739.6SLC13A2-2041230No protein-
 
Retained intron
--TSL:2
Statistics

Exons: 12, Coding exons: 12, Transcript length: 2,360 bps, Translation length: 592 residues

MANE

This MANE Select transcript contains ENSP00000316202 and matches to NM_003984.4 and NP_003975.1

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q13183

CCDS

This transcript is a member of the Human CCDS set: CCDS11231

Transcript Support Level (TSL)

TSL:1

Version

ENST00000314669.10

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.