Canonical Allele Identifier: CA490017486

Gene: SLC12A1

Linked Data

• MyVariant Identifiers: chr15:g.48527132T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48234935T>C , CM000677.2:g.48234935T>C	GRCh38
NC_000015.9:g.48527132T>C , CM000677.1:g.48527132T>C	GRCh37
NC_000015.8:g.46314424T>C	NCBI36
NG_021301.1:g.33635T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000686073.1:c.1146T>C	ENSP00000508901.1:p.Ser382=
ENST00000380993.8:c.1146T>C MANE Select	ENSP00000370381.3:p.Ser382=
ENST00000646012.1:c.1284T>C	ENSP00000495813.1:p.Ser428=
ENST00000647232.1:c.1146T>C	ENSP00000493875.1:p.Ser382=
ENST00000647546.1:c.1146T>C	ENSP00000495332.1:p.Ser382=
ENST00000330289.10:c.1146T>C	ENSP00000331550.6:p.Ser382=
ENST00000380993.7:c.1146T>C	ENSP00000370381.3:p.Ser382=
ENST00000396577.7:c.1146T>C	ENSP00000379822.3:p.Ser382=
ENST00000558252.5:n.5269T>C
ENST00000558405.5:c.1146T>C	ENSP00000453409.1:p.Ser382=
ENST00000558805.1:c.173T>C
ENST00000559641.5:c.585T>C	ENSP00000453230.1:p.Ser195=
ENST00000560692.5:n.5285T>C
NM_000338.2:c.1146T>C	NP_000329.2:p.Ser382=
NM_001184832.1:c.1146T>C	NP_001171761.1:p.Ser382=
XM_005254605.1:c.1242T>C	XP_005254662.1:p.Ser414=
XM_005254606.1:c.1146T>C	XP_005254663.1:p.Ser382=
XM_006720656.1:c.1242T>C	XP_006720719.1:p.Ser414=
XR_931896.1:n.1458T>C
XM_005254606.2:c.1146T>C	XP_005254663.1:p.Ser382=
NM_000338.3:c.1146T>C MANE Select	NP_000329.2:p.Ser382=
NM_001184832.2:c.1146T>C	NP_001171761.1:p.Ser382=
NM_001384136.1:c.1146T>C	NP_001371065.1:p.Ser382=