Canonical Allele Identifier: CA2224349095

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56869768C= , CM000678.2:g.56869768C=	GRCh38
NC_000016.9:g.56903680C= , CM000678.1:g.56903680C=	GRCh37
NC_000016.8:g.55461181C=	NCBI36
NG_009386.1:g.9562C=
NG_009386.2:g.9562C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.545C= MANE Select	ENSP00000456149.2:p.Thr182=
ENST00000262502.5:c.542C=	ENSP00000262502.5:p.Thr181=
ENST00000438926.6:c.545C=	ENSP00000402152.2:p.Thr182=
ENST00000563236.5:c.545C=	ENSP00000456149.1:p.Thr182=
ENST00000566786.5:c.542C=	ENSP00000457552.1:p.Thr181=
NM_000339.2:c.545C=	NP_000330.2:p.Thr182=
NM_001126107.1:c.542C=	NP_001119579.1:p.Thr181=
NM_001126108.1:c.545C=	NP_001119580.1:p.Thr182=
XM_005256119.1:c.542C=	XP_005256176.1:p.Thr181=
XM_005256119.2:c.542C=	XP_005256176.1:p.Thr181=
NM_000339.3:c.545C=	NP_000330.3:p.Thr182=
NM_001126107.2:c.542C=	NP_001119579.2:p.Thr181=
NM_001126108.2:c.545C= MANE Select	NP_001119580.2:p.Thr182=