Canonical Allele Identifier: CA392306828

Gene: SLC12A1

Linked Data

• COSMIC: COSM4055263 ; COSM4055264
• MyVariant Identifiers: chr15:g.48521412A>C (hg19) ; chr15:g.48229215A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48229215A>C , CM000677.2:g.48229215A>C	GRCh38
NC_000015.9:g.48521412A>C , CM000677.1:g.48521412A>C	GRCh37
NC_000015.8:g.46308704A>C	NCBI36
NG_021301.1:g.27915A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000686073.1:c.751A>C	ENSP00000508901.1:p.Ser251Arg
ENST00000380993.8:c.751A>C MANE Select	ENSP00000370381.3:p.Ser251Arg
ENST00000646012.1:c.889A>C	ENSP00000495813.1:p.Ser297Arg
ENST00000647232.1:c.751A>C	ENSP00000493875.1:p.Ser251Arg
ENST00000647546.1:c.751A>C	ENSP00000495332.1:p.Ser251Arg
ENST00000330289.10:c.751A>C	ENSP00000331550.6:p.Ser251Arg
ENST00000380993.7:c.751A>C	ENSP00000370381.3:p.Ser251Arg
ENST00000396577.7:c.751A>C	ENSP00000379822.3:p.Ser251Arg
ENST00000558252.5:n.4874A>C
ENST00000558405.5:c.751A>C	ENSP00000453409.1:p.Ser251Arg
ENST00000559641.5:c.190A>C	ENSP00000453230.1:p.Ser64Arg
ENST00000559723.2:n.124A>C
ENST00000560692.5:n.4890A>C
ENST00000561127.5:c.190A>C	ENSP00000453602.2:p.Ser64Arg
NM_000338.2:c.751A>C	NP_000329.2:p.Ser251Arg
NM_001184832.1:c.751A>C	NP_001171761.1:p.Ser251Arg
XM_005254605.1:c.847A>C	XP_005254662.1:p.Ser283Arg
XM_005254606.1:c.751A>C	XP_005254663.1:p.Ser251Arg
XM_006720656.1:c.847A>C	XP_006720719.1:p.Ser283Arg
XR_931896.1:n.1063A>C
XR_932203.1:n.229+741T>G
XR_932204.1:n.222+741T>G
XM_005254606.2:c.751A>C	XP_005254663.1:p.Ser251Arg
XR_001751524.2:n.230+741T>G
XR_001751525.1:n.230+741T>G
XR_002957762.1:n.230+741T>G
XR_932204.3:n.224+741T>G
NM_000338.3:c.751A>C MANE Select	NP_000329.2:p.Ser251Arg
NM_001184832.2:c.751A>C	NP_001171761.1:p.Ser251Arg
NM_001384136.1:c.751A>C	NP_001371065.1:p.Ser251Arg