Canonical Allele Identifier: CA2224364846

Gene: SLC12A3

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56902492C= , CM000678.2:g.56902492C=	GRCh38
NC_000016.9:g.56936404C= , CM000678.1:g.56936404C=	GRCh37
NC_000016.8:g.55493905C=	NCBI36
NG_009386.1:g.42286C=
NG_009386.2:g.42286C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000563236.6:c.2840C= MANE Select	ENSP00000456149.2:p.Thr947=
ENST00000262502.5:c.2837C=	ENSP00000262502.5:p.Thr946=
ENST00000438926.6:c.2867C=	ENSP00000402152.2:p.Thr956=
ENST00000563236.5:c.2840C=	ENSP00000456149.1:p.Thr947=
ENST00000566786.5:c.2864C=	ENSP00000457552.1:p.Thr955=
ENST00000569002.1:n.271C=
NM_000339.2:c.2867C=	NP_000330.2:p.Thr956=
NM_001126107.1:c.2864C=	NP_001119579.1:p.Thr955=
NM_001126108.1:c.2840C=	NP_001119580.1:p.Thr947=
XM_005256119.1:c.2837C=	XP_005256176.1:p.Thr946=
XM_005256119.2:c.2837C=	XP_005256176.1:p.Thr946=
NM_000339.3:c.2867C=	NP_000330.3:p.Thr956=
NM_001126107.2:c.2864C=	NP_001119579.2:p.Thr955=
NM_001126108.2:c.2840C= MANE Select	NP_001119580.2:p.Thr947=