Canonical Allele Identifier: CA229599044

Gene: SLC37A4

Linked Data

• dbSNP Id: rs5795159
• COSMIC: COSM6368870
• MyVariant Identifiers: chr11:g.118898436C>A (hg19) ; chr11:g.119027726C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119027726C>A , CM000673.2:g.119027726C>A	GRCh38
NC_000011.9:g.118898436C>A , CM000673.1:g.118898436C>A	GRCh37
NC_000011.8:g.118403646C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000529510.6:n.757G>T
ENST00000697845.1:n.681G>T
ENST00000697846.1:n.757G>T
ENST00000697847.1:n.757G>T
ENST00000697848.1:n.757G>T
ENST00000697849.1:n.1796G>T
ENST00000697850.1:n.757G>T
ENST00000697851.1:n.2117G>T
ENST00000638186.1:n.831G>T
ENST00000638360.1:n.663G>T
ENST00000638925.1:n.764G>T
ENST00000650539.1:n.933G>T
ENST00000330775.9:c.528G>T	ENSP00000476242.2:p.Trp176Cys
ENST00000357590.9:c.528G>T	ENSP00000476176.2:p.Trp176Cys
ENST00000524428.5:n.849G>T
ENST00000525039.5:n.951G>T
ENST00000525102.5:n.1285G>T
ENST00000525372.5:n.528G>T
ENST00000526275.5:n.1309G>T
ENST00000526626.6:n.490G>T
ENST00000527992.5:n.755G>T
ENST00000529510.5:n.399+468G>T
ENST00000530407.5:n.677G>T
ENST00000532085.1:n.3138G>T
ENST00000532888.6:n.823G>T
ENST00000538950.5:c.309G>T	ENSP00000475991.2:p.Trp103Cys
ENST00000545985.5:c.528G>T	ENSP00000475241.2:p.Trp176Cys