Canonical Allele Identifier: CA1581197811

Gene: SLC12A2

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186784T= , CM000667.2:g.128186784T=	GRCh38
NC_000005.9:g.127522476T= , CM000667.1:g.127522476T=	GRCh37
NC_000005.8:g.127550375T=	NCBI36
NG_042286.1:g.107994T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.*153T= MANE Select	ENSP00000262461.2:n.*153T=
ENST00000262461.6:c.*153T=	ENSP00000262461.2:n.*153T=
ENST00000343225.4:c.*153T=	ENSP00000340878.4:n.*153T=
ENST00000509205.5:c.*405T=	ENSP00000427109.1:n.*405T=
NM_001046.2:c.*153T=	NP_001037.1:n.*153T=
NM_001256461.1:c.*153T=	NP_001243390.1:n.*153T=
NR_046207.1:n.4022T=
XM_017009771.1:c.*153T=	XP_016865260.1:n.*153T=
XR_001742214.1:n.4016T=
NM_001046.3:c.*153T= MANE Select	NP_001037.1:n.*153T=
NM_001256461.2:c.*153T=	NP_001243390.1:n.*153T=
NR_046207.2:n.4047T=