Canonical Allele Identifier: CA360743375

Gene: SLC12A2

Linked Data

• MyVariant Identifiers: chr5:g.127522309A>G (hg19) ; chr5:g.128186617A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186617A>G , CM000667.2:g.128186617A>G	GRCh38
NC_000005.9:g.127522309A>G , CM000667.1:g.127522309A>G	GRCh37
NC_000005.8:g.127550208A>G	NCBI36
NG_042286.1:g.107827A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3625A>G MANE Select	ENSP00000262461.2:p.Thr1209Ala
ENST00000262461.6:c.3625A>G	ENSP00000262461.2:p.Thr1209Ala
ENST00000343225.4:c.3577A>G	ENSP00000340878.4:p.Thr1193Ala
ENST00000509205.5:c.*238A>G	ENSP00000427109.1:n.*238A>G
NM_001046.2:c.3625A>G	NP_001037.1:p.Thr1209Ala
NM_001256461.1:c.3577A>G	NP_001243390.1:p.Thr1193Ala
NR_046207.1:n.3855A>G
XM_017009771.1:c.1867A>G	XP_016865260.1:p.Thr623Ala
XR_001742214.1:n.3849A>G
NM_001046.3:c.3625A>G MANE Select	NP_001037.1:p.Thr1209Ala
NM_001256461.2:c.3577A>G	NP_001243390.1:p.Thr1193Ala
NR_046207.2:n.3880A>G