Canonical Allele Identifier: CA392308606

Gene: SLC12A1

Linked Data

• dbSNP Id: rs2141040187
• MyVariant Identifiers: chr15:g.48527134T>C (hg19) ; chr15:g.48234937T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48234937T>C , CM000677.2:g.48234937T>C	GRCh38
NC_000015.9:g.48527134T>C , CM000677.1:g.48527134T>C	GRCh37
NC_000015.8:g.46314426T>C	NCBI36
NG_021301.1:g.33637T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000686073.1:c.1148T>C	ENSP00000508901.1:p.Val383Ala
ENST00000380993.8:c.1148T>C MANE Select	ENSP00000370381.3:p.Val383Ala
ENST00000646012.1:c.1286T>C	ENSP00000495813.1:p.Val429Ala
ENST00000647232.1:c.1148T>C	ENSP00000493875.1:p.Val383Ala
ENST00000647546.1:c.1148T>C	ENSP00000495332.1:p.Val383Ala
ENST00000330289.10:c.1148T>C	ENSP00000331550.6:p.Val383Ala
ENST00000380993.7:c.1148T>C	ENSP00000370381.3:p.Val383Ala
ENST00000396577.7:c.1148T>C	ENSP00000379822.3:p.Val383Ala
ENST00000558252.5:n.5271T>C
ENST00000558405.5:c.1148T>C	ENSP00000453409.1:p.Val383Ala
ENST00000558805.1:c.175T>C
ENST00000559641.5:c.587T>C	ENSP00000453230.1:p.Val196Ala
ENST00000560692.5:n.5287T>C
NM_000338.2:c.1148T>C	NP_000329.2:p.Val383Ala
NM_001184832.1:c.1148T>C	NP_001171761.1:p.Val383Ala
XM_005254605.1:c.1244T>C	XP_005254662.1:p.Val415Ala
XM_005254606.1:c.1148T>C	XP_005254663.1:p.Val383Ala
XM_006720656.1:c.1244T>C	XP_006720719.1:p.Val415Ala
XR_931896.1:n.1460T>C
XM_005254606.2:c.1148T>C	XP_005254663.1:p.Val383Ala
NM_000338.3:c.1148T>C MANE Select	NP_000329.2:p.Val383Ala
NM_001184832.2:c.1148T>C	NP_001171761.1:p.Val383Ala
NM_001384136.1:c.1148T>C	NP_001371065.1:p.Val383Ala