Canonical Allele Identifier: CA1581197589

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186575C= , CM000667.2:g.128186575C=	GRCh38
NC_000005.9:g.127522267C= , CM000667.1:g.127522267C=	GRCh37
NC_000005.8:g.127550166C=	NCBI36
NG_042286.1:g.107785C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3583C= MANE Select	ENSP00000262461.2:p.Pro1195=
ENST00000262461.6:c.3583C=	ENSP00000262461.2:p.Pro1195=
ENST00000343225.4:c.3535C=	ENSP00000340878.4:p.Pro1179=
ENST00000509205.5:c.*196C=	ENSP00000427109.1:n.*196C=
NM_001046.2:c.3583C=	NP_001037.1:p.Pro1195=
NM_001256461.1:c.3535C=	NP_001243390.1:p.Pro1179=
NR_046207.1:n.3813C=
XM_017009771.1:c.1825C=	XP_016865260.1:p.Pro609=
XR_001742214.1:n.3807C=
NM_001046.3:c.3583C= MANE Select	NP_001037.1:p.Pro1195=
NM_001256461.2:c.3535C=	NP_001243390.1:p.Pro1179=
NR_046207.2:n.3838C=