Human (GRCh38.p14)
Description

solute carrier family 18 member A2 [Source:HGNC Symbol;Acc:HGNC:10935]

Gene Synonyms

SVAT, SVMT, VAT2, VMAT2

Location

Chromosome 10: 117,240,830-117,279,430 forward strand.

GRCh38:CM000672.2

About this gene

This gene has 10 transcripts (splice variants), 222 orthologues, 3 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000644641.2SLC18A2-2023831514aaENSP00000496339.1
 
Protein coding
CCDS7599Q05940-1 NM_003054.6MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000921156.1SLC18A2-2064573514aaENSP00000591215.1
 
Protein coding
CCDS7599--GENCODE PrimaryGENCODE BasicAPPRIS P1
ENST00000956273.1SLC18A2-2104027514aaENSP00000626332.1
 
Protein coding
CCDS7599--GENCODE BasicAPPRIS P1
ENST00000921157.1SLC18A2-2074025484aaENSP00000591216.1
 
Protein coding
--GENCODE Basic
ENST00000853677.1SLC18A2-2033927546aaENSP00000523736.1
 
Protein coding
--GENCODE Basic
ENST00000921158.1SLC18A2-2083621456aaENSP00000591217.1
 
Protein coding
--GENCODE Basic
ENST00000853679.1SLC18A2-2052754545aaENSP00000523738.1
 
Protein coding
--GENCODE Basic
ENST00000853678.1SLC18A2-2042625482aaENSP00000523737.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000921159.1SLC18A2-2092157483aaENSP00000591218.1
 
Protein coding
--GENCODE Basic
ENST00000497497.1SLC18A2-2014125No protein-
 
Retained intron
--TSL:2