Canonical Allele Identifier: CA1581197662

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186652C= , CM000667.2:g.128186652C=	GRCh38
NC_000005.9:g.127522344C= , CM000667.1:g.127522344C=	GRCh37
NC_000005.8:g.127550243C=	NCBI36
NG_042286.1:g.107862C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*21C= MANE Select	ENSP00000262461.2:n.*21C=
ENST00000262461.6:c.*21C=	ENSP00000262461.2:n.*21C=
ENST00000343225.4:c.*21C=	ENSP00000340878.4:n.*21C=
ENST00000509205.5:c.*273C=	ENSP00000427109.1:n.*273C=
NM_001046.2:c.*21C=	NP_001037.1:n.*21C=
NM_001256461.1:c.*21C=	NP_001243390.1:n.*21C=
NR_046207.1:n.3890C=
XM_017009771.1:c.*21C=	XP_016865260.1:n.*21C=
XR_001742214.1:n.3884C=
NM_001046.3:c.*21C= MANE Select	NP_001037.1:n.*21C=
NM_001256461.2:c.*21C=	NP_001243390.1:n.*21C=
NR_046207.2:n.3915C=