Human (GRCh38.p14)
Description

solute carrier family 5 member 2 [Source:HGNC Symbol;Acc:HGNC:11037]

Gene Synonyms

SGLT2

Location
About this transcript

This transcript has 2 exons, is associated with 840 variant alleles and maps to 59 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000330498.4SLC5A2-2012267672aaENSP00000327943.3
 
Protein coding
CCDS10714P31639-1 NM_003041.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:1
ENST00000569576.5SLC5A2-209516148aaENSP00000455143.1
 
Protein coding
H3BP44 -TSL:4CDS 3' incomplete
ENST00000419665.6SLC5A2-2021852458aaENSP00000410601.2
 
Nonsense mediated decay
P31639-2 -TSL:1
ENST00000564197.1SLC5A2-204498No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000567051.1SLC5A2-206334No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000568188.1SLC5A2-2072467No protein-
 
Retained intron
--TSL:2
ENST00000562006.1SLC5A2-203995No protein-
 
Retained intron
--TSL:3
ENST00000568891.1SLC5A2-208660No protein-
 
Retained intron
--TSL:5
ENST00000565446.1SLC5A2-205449No protein-
 
Retained intron
--TSL:5
Statistics

Exons: 2, Coding exons: 0, Transcript length: 498 bps,

Transcript Support Level (TSL)

TSL:5

Version

ENST00000564197.1

Type

Protein coding CDS not defined

Annotation Method

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