Canonical Allele Identifier: CA392308502

Gene: SLC12A1

Linked Data

• COSMIC: COSM4055269 ; COSM4055270
• MyVariant Identifiers: chr15:g.48527094T>G (hg19) ; chr15:g.48234897T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48234897T>G , CM000677.2:g.48234897T>G	GRCh38
NC_000015.9:g.48527094T>G , CM000677.1:g.48527094T>G	GRCh37
NC_000015.8:g.46314386T>G	NCBI36
NG_021301.1:g.33597T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686073.1:c.1108T>G	ENSP00000508901.1:p.Phe370Val
ENST00000380993.8:c.1108T>G MANE Select	ENSP00000370381.3:p.Phe370Val
ENST00000646012.1:c.1246T>G	ENSP00000495813.1:p.Phe416Val
ENST00000647232.1:c.1108T>G	ENSP00000493875.1:p.Phe370Val
ENST00000647546.1:c.1108T>G	ENSP00000495332.1:p.Phe370Val
ENST00000330289.10:c.1108T>G	ENSP00000331550.6:p.Phe370Val
ENST00000380993.7:c.1108T>G	ENSP00000370381.3:p.Phe370Val
ENST00000396577.7:c.1108T>G	ENSP00000379822.3:p.Phe370Val
ENST00000558252.5:n.5231T>G
ENST00000558405.5:c.1108T>G	ENSP00000453409.1:p.Phe370Val
ENST00000558805.1:c.135T>G
ENST00000559641.5:c.547T>G	ENSP00000453230.1:p.Phe183Val
ENST00000559723.2:n.481T>G
ENST00000560692.5:n.5247T>G
NM_000338.2:c.1108T>G	NP_000329.2:p.Phe370Val
NM_001184832.1:c.1108T>G	NP_001171761.1:p.Phe370Val
XM_005254605.1:c.1204T>G	XP_005254662.1:p.Phe402Val
XM_005254606.1:c.1108T>G	XP_005254663.1:p.Phe370Val
XM_006720656.1:c.1204T>G	XP_006720719.1:p.Phe402Val
XR_931896.1:n.1420T>G
XM_005254606.2:c.1108T>G	XP_005254663.1:p.Phe370Val
NM_000338.3:c.1108T>G MANE Select	NP_000329.2:p.Phe370Val
NM_001184832.2:c.1108T>G	NP_001171761.1:p.Phe370Val
NM_001384136.1:c.1108T>G	NP_001371065.1:p.Phe370Val