Canonical Allele Identifier: CA2224365739

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56904429T= , CM000678.2:g.56904429T=	GRCh38
NC_000016.9:g.56938341T= , CM000678.1:g.56938341T=	GRCh37
NC_000016.8:g.55495842T=	NCBI36
NG_009386.1:g.44223T=
NG_009386.2:g.44223T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2891T= MANE Select	ENSP00000456149.2:p.Leu964=
ENST00000262502.5:c.2888T=	ENSP00000262502.5:p.Leu963=
ENST00000438926.6:c.2918T=	ENSP00000402152.2:p.Leu973=
ENST00000563236.5:c.2891T=	ENSP00000456149.1:p.Leu964=
ENST00000566786.5:c.2915T=	ENSP00000457552.1:p.Leu972=
ENST00000569002.1:n.322T=
NM_000339.2:c.2918T=	NP_000330.2:p.Leu973=
NM_001126107.1:c.2915T=	NP_001119579.1:p.Leu972=
NM_001126108.1:c.2891T=	NP_001119580.1:p.Leu964=
XM_005256119.1:c.2888T=	XP_005256176.1:p.Leu963=
XM_005256119.2:c.2888T=	XP_005256176.1:p.Leu963=
NM_000339.3:c.2918T=	NP_000330.3:p.Leu973=
NM_001126107.2:c.2915T=	NP_001119579.2:p.Leu972=
NM_001126108.2:c.2891T= MANE Select	NP_001119580.2:p.Leu964=