Canonical Allele Identifier: CA1581197648

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186641A= , CM000667.2:g.128186641A=	GRCh38
NC_000005.9:g.127522333A= , CM000667.1:g.127522333A=	GRCh37
NC_000005.8:g.127550232A=	NCBI36
NG_042286.1:g.107851A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*10A= MANE Select	ENSP00000262461.2:n.*10A=
ENST00000262461.6:c.*10A=	ENSP00000262461.2:n.*10A=
ENST00000343225.4:c.*10A=	ENSP00000340878.4:n.*10A=
ENST00000509205.5:c.*262A=	ENSP00000427109.1:n.*262A=
NM_001046.2:c.*10A=	NP_001037.1:n.*10A=
NM_001256461.1:c.*10A=	NP_001243390.1:n.*10A=
NR_046207.1:n.3879A=
XM_017009771.1:c.*10A=	XP_016865260.1:n.*10A=
XR_001742214.1:n.3873A=
NM_001046.3:c.*10A= MANE Select	NP_001037.1:n.*10A=
NM_001256461.2:c.*10A=	NP_001243390.1:n.*10A=
NR_046207.2:n.3904A=