Canonical Allele Identifier: CA2224365748

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56904444A= , CM000678.2:g.56904444A=	GRCh38
NC_000016.9:g.56938356A= , CM000678.1:g.56938356A=	GRCh37
NC_000016.8:g.55495857A=	NCBI36
NG_009386.1:g.44238A=
NG_009386.2:g.44238A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2906A= MANE Select	ENSP00000456149.2:p.Asp969=
ENST00000262502.5:c.2903A=	ENSP00000262502.5:p.Asp968=
ENST00000438926.6:c.2933A=	ENSP00000402152.2:p.Asp978=
ENST00000563236.5:c.2906A=	ENSP00000456149.1:p.Asp969=
ENST00000566786.5:c.2930A=	ENSP00000457552.1:p.Asp977=
ENST00000569002.1:n.337A=
NM_000339.2:c.2933A=	NP_000330.2:p.Asp978=
NM_001126107.1:c.2930A=	NP_001119579.1:p.Asp977=
NM_001126108.1:c.2906A=	NP_001119580.1:p.Asp969=
XM_005256119.1:c.2903A=	XP_005256176.1:p.Asp968=
XM_005256119.2:c.2903A=	XP_005256176.1:p.Asp968=
NM_000339.3:c.2933A=	NP_000330.3:p.Asp978=
NM_001126107.2:c.2930A=	NP_001119579.2:p.Asp977=
NM_001126108.2:c.2906A= MANE Select	NP_001119580.2:p.Asp969=