Canonical Allele Identifier: CA1581197817

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186794G= , CM000667.2:g.128186794G=	GRCh38
NC_000005.9:g.127522486G= , CM000667.1:g.127522486G=	GRCh37
NC_000005.8:g.127550385G=	NCBI36
NG_042286.1:g.108004G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*163G= MANE Select	ENSP00000262461.2:n.*163G=
ENST00000262461.6:c.*163G=	ENSP00000262461.2:n.*163G=
ENST00000343225.4:c.*163G=	ENSP00000340878.4:n.*163G=
ENST00000509205.5:c.*415G=	ENSP00000427109.1:n.*415G=
NM_001046.2:c.*163G=	NP_001037.1:n.*163G=
NM_001256461.1:c.*163G=	NP_001243390.1:n.*163G=
NR_046207.1:n.4032G=
XM_017009771.1:c.*163G=	XP_016865260.1:n.*163G=
XR_001742214.1:n.4026G=
NM_001046.3:c.*163G= MANE Select	NP_001037.1:n.*163G=
NM_001256461.2:c.*163G=	NP_001243390.1:n.*163G=
NR_046207.2:n.4057G=