Canonical Allele Identifier: CA1581197690

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186672G= , CM000667.2:g.128186672G=	GRCh38
NC_000005.9:g.127522364G= , CM000667.1:g.127522364G=	GRCh37
NC_000005.8:g.127550263G=	NCBI36
NG_042286.1:g.107882G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*41G= MANE Select	ENSP00000262461.2:n.*41G=
ENST00000262461.6:c.*41G=	ENSP00000262461.2:n.*41G=
ENST00000343225.4:c.*41G=	ENSP00000340878.4:n.*41G=
ENST00000509205.5:c.*293G=	ENSP00000427109.1:n.*293G=
NM_001046.2:c.*41G=	NP_001037.1:n.*41G=
NM_001256461.1:c.*41G=	NP_001243390.1:n.*41G=
NR_046207.1:n.3910G=
XM_017009771.1:c.*41G=	XP_016865260.1:n.*41G=
XR_001742214.1:n.3904G=
NM_001046.3:c.*41G= MANE Select	NP_001037.1:n.*41G=
NM_001256461.2:c.*41G=	NP_001243390.1:n.*41G=
NR_046207.2:n.3935G=