Canonical Allele Identifier: CA1581197550

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186556A= , CM000667.2:g.128186556A=	GRCh38
NC_000005.9:g.127522248A= , CM000667.1:g.127522248A=	GRCh37
NC_000005.8:g.127550147A=	NCBI36
NG_042286.1:g.107766A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3564A= MANE Select	ENSP00000262461.2:p.Glu1188=
ENST00000262461.6:c.3564A=	ENSP00000262461.2:p.Glu1188=
ENST00000343225.4:c.3516A=	ENSP00000340878.4:p.Glu1172=
ENST00000509205.5:c.*177A=	ENSP00000427109.1:n.*177A=
NM_001046.2:c.3564A=	NP_001037.1:p.Glu1188=
NM_001256461.1:c.3516A=	NP_001243390.1:p.Glu1172=
NR_046207.1:n.3794A=
XM_017009771.1:c.1806A=	XP_016865260.1:p.Glu602=
XR_001742214.1:n.3788A=
NM_001046.3:c.3564A= MANE Select	NP_001037.1:p.Glu1188=
NM_001256461.2:c.3516A=	NP_001243390.1:p.Glu1172=
NR_046207.2:n.3819A=