Canonical Allele Identifier: CA1581197805

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186780T= , CM000667.2:g.128186780T=	GRCh38
NC_000005.9:g.127522472T= , CM000667.1:g.127522472T=	GRCh37
NC_000005.8:g.127550371T=	NCBI36
NG_042286.1:g.107990T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*149T= MANE Select	ENSP00000262461.2:n.*149T=
ENST00000262461.6:c.*149T=	ENSP00000262461.2:n.*149T=
ENST00000343225.4:c.*149T=	ENSP00000340878.4:n.*149T=
ENST00000509205.5:c.*401T=	ENSP00000427109.1:n.*401T=
NM_001046.2:c.*149T=	NP_001037.1:n.*149T=
NM_001256461.1:c.*149T=	NP_001243390.1:n.*149T=
NR_046207.1:n.4018T=
XM_017009771.1:c.*149T=	XP_016865260.1:n.*149T=
XR_001742214.1:n.4012T=
NM_001046.3:c.*149T= MANE Select	NP_001037.1:n.*149T=
NM_001256461.2:c.*149T=	NP_001243390.1:n.*149T=
NR_046207.2:n.4043T=