Canonical Allele Identifier: CA2175391448

Gene: SLC12A1

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.48226557G= , CM000677.2:g.48226557G=	GRCh38
NC_000015.9:g.48518754G= , CM000677.1:g.48518754G=	GRCh37
NC_000015.8:g.46306046G=	NCBI36
NG_021301.1:g.25257G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686073.1:c.724+610G=	ENSP00000508901.1:n.724+610G=
ENST00000380993.8:c.710G= MANE Select	ENSP00000370381.3:p.Gly237=
ENST00000646012.1:c.848G=	ENSP00000495813.1:p.Gly283=
ENST00000647232.1:c.629-522G=	ENSP00000493875.1:n.629-522G=
ENST00000647546.1:c.710G=	ENSP00000495332.1:p.Gly237=
ENST00000330289.10:c.710G=	ENSP00000331550.6:p.Gly237=
ENST00000380993.7:c.710G=	ENSP00000370381.3:p.Gly237=
ENST00000396577.7:c.629-522G=	ENSP00000379822.3:n.629-522G=
ENST00000558252.5:n.4230G=
ENST00000558405.5:c.710G=	ENSP00000453409.1:p.Gly237=
ENST00000559641.5:c.149G=	ENSP00000453230.1:p.Gly50=
ENST00000559723.2:n.97+610G=
ENST00000560692.5:n.2232G=
ENST00000561127.5:c.149G=	ENSP00000453602.2:p.Gly50=
NM_000338.2:c.710G=	NP_000329.2:p.Gly237=
NM_001184832.1:c.629-522G=	NP_001171761.1:n.629-522G=
XM_005254605.1:c.710G=	XP_005254662.1:p.Gly237=
XM_005254606.1:c.724+610G=	XP_005254663.1:n.724+610G=
XM_006720656.1:c.710G=	XP_006720719.1:p.Gly237=
XR_931896.1:n.926G=
XM_005254606.2:c.724+610G=	XP_005254663.1:n.724+610G=
XR_001751524.2:n.363+904C=
XR_001751525.1:n.363+904C=
XR_002957762.1:n.363+904C=
XR_932204.3:n.357+904C=
NM_000338.3:c.710G= MANE Select	NP_000329.2:p.Gly237=
NM_001184832.2:c.629-522G=	NP_001171761.1:n.629-522G=
NM_001384136.1:c.724+610G=	NP_001371065.1:n.724+610G=