Canonical Allele Identifier: CA1581197676

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186661A= , CM000667.2:g.128186661A=	GRCh38
NC_000005.9:g.127522353A= , CM000667.1:g.127522353A=	GRCh37
NC_000005.8:g.127550252A=	NCBI36
NG_042286.1:g.107871A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000262461.7:c.*30A= MANE Select	ENSP00000262461.2:n.*30A=
ENST00000262461.6:c.*30A=	ENSP00000262461.2:n.*30A=
ENST00000343225.4:c.*30A=	ENSP00000340878.4:n.*30A=
ENST00000509205.5:c.*282A=	ENSP00000427109.1:n.*282A=
NM_001046.2:c.*30A=	NP_001037.1:n.*30A=
NM_001256461.1:c.*30A=	NP_001243390.1:n.*30A=
NR_046207.1:n.3899A=
XM_017009771.1:c.*30A=	XP_016865260.1:n.*30A=
XR_001742214.1:n.3893A=
NM_001046.3:c.*30A= MANE Select	NP_001037.1:n.*30A=
NM_001256461.2:c.*30A=	NP_001243390.1:n.*30A=
NR_046207.2:n.3924A=