Canonical Allele Identifier: CA490017497

Gene: SLC12A1

Linked Data

• MyVariant Identifiers: chr15:g.48527135C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48234938C>A , CM000677.2:g.48234938C>A	GRCh38
NC_000015.9:g.48527135C>A , CM000677.1:g.48527135C>A	GRCh37
NC_000015.8:g.46314427C>A	NCBI36
NG_021301.1:g.33638C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000686073.1:c.1149C>A	ENSP00000508901.1:p.Val383=
ENST00000380993.8:c.1149C>A MANE Select	ENSP00000370381.3:p.Val383=
ENST00000646012.1:c.1287C>A	ENSP00000495813.1:p.Val429=
ENST00000647232.1:c.1149C>A	ENSP00000493875.1:p.Val383=
ENST00000647546.1:c.1149C>A	ENSP00000495332.1:p.Val383=
ENST00000330289.10:c.1149C>A	ENSP00000331550.6:p.Val383=
ENST00000380993.7:c.1149C>A	ENSP00000370381.3:p.Val383=
ENST00000396577.7:c.1149C>A	ENSP00000379822.3:p.Val383=
ENST00000558252.5:n.5272C>A
ENST00000558405.5:c.1149C>A	ENSP00000453409.1:p.Val383=
ENST00000558805.1:c.176C>A
ENST00000559641.5:c.588C>A	ENSP00000453230.1:p.Val196=
ENST00000560692.5:n.5288C>A
NM_000338.2:c.1149C>A	NP_000329.2:p.Val383=
NM_001184832.1:c.1149C>A	NP_001171761.1:p.Val383=
XM_005254605.1:c.1245C>A	XP_005254662.1:p.Val415=
XM_005254606.1:c.1149C>A	XP_005254663.1:p.Val383=
XM_006720656.1:c.1245C>A	XP_006720719.1:p.Val415=
XR_931896.1:n.1461C>A
XM_005254606.2:c.1149C>A	XP_005254663.1:p.Val383=
NM_000338.3:c.1149C>A MANE Select	NP_000329.2:p.Val383=
NM_001184832.2:c.1149C>A	NP_001171761.1:p.Val383=
NM_001384136.1:c.1149C>A	NP_001371065.1:p.Val383=