Canonical Allele Identifier: CA1581197594

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186578C= , CM000667.2:g.128186578C=	GRCh38
NC_000005.9:g.127522270C= , CM000667.1:g.127522270C=	GRCh37
NC_000005.8:g.127550169C=	NCBI36
NG_042286.1:g.107788C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3586C= MANE Select	ENSP00000262461.2:p.Pro1196=
ENST00000262461.6:c.3586C=	ENSP00000262461.2:p.Pro1196=
ENST00000343225.4:c.3538C=	ENSP00000340878.4:p.Pro1180=
ENST00000509205.5:c.*199C=	ENSP00000427109.1:n.*199C=
NM_001046.2:c.3586C=	NP_001037.1:p.Pro1196=
NM_001256461.1:c.3538C=	NP_001243390.1:p.Pro1180=
NR_046207.1:n.3816C=
XM_017009771.1:c.1828C=	XP_016865260.1:p.Pro610=
XR_001742214.1:n.3810C=
NM_001046.3:c.3586C= MANE Select	NP_001037.1:p.Pro1196=
NM_001256461.2:c.3538C=	NP_001243390.1:p.Pro1180=
NR_046207.2:n.3841C=