Canonical Allele Identifier: CA360743378

Gene: SLC12A2

Linked Data

• MyVariant Identifiers: chr5:g.127522310C>A (hg19) ; chr5:g.128186618C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186618C>A , CM000667.2:g.128186618C>A	GRCh38
NC_000005.9:g.127522310C>A , CM000667.1:g.127522310C>A	GRCh37
NC_000005.8:g.127550209C>A	NCBI36
NG_042286.1:g.107828C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3626C>A MANE Select	ENSP00000262461.2:p.Thr1209Asn
ENST00000262461.6:c.3626C>A	ENSP00000262461.2:p.Thr1209Asn
ENST00000343225.4:c.3578C>A	ENSP00000340878.4:p.Thr1193Asn
ENST00000509205.5:c.*239C>A	ENSP00000427109.1:n.*239C>A
NM_001046.2:c.3626C>A	NP_001037.1:p.Thr1209Asn
NM_001256461.1:c.3578C>A	NP_001243390.1:p.Thr1193Asn
NR_046207.1:n.3856C>A
XM_017009771.1:c.1868C>A	XP_016865260.1:p.Thr623Asn
XR_001742214.1:n.3850C>A
NM_001046.3:c.3626C>A MANE Select	NP_001037.1:p.Thr1209Asn
NM_001256461.2:c.3578C>A	NP_001243390.1:p.Thr1193Asn
NR_046207.2:n.3881C>A