Canonical Allele Identifier: CA360743334

Gene: SLC12A2

Linked Data

• MyVariant Identifiers: chr5:g.127522301G>C (hg19) ; chr5:g.128186609G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.128186609G>C , CM000667.2:g.128186609G>C	GRCh38
NC_000005.9:g.127522301G>C , CM000667.1:g.127522301G>C	GRCh37
NC_000005.8:g.127550200G>C	NCBI36
NG_042286.1:g.107819G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262461.7:c.3617G>C MANE Select	ENSP00000262461.2:p.Ser1206Thr
ENST00000262461.6:c.3617G>C	ENSP00000262461.2:p.Ser1206Thr
ENST00000343225.4:c.3569G>C	ENSP00000340878.4:p.Ser1190Thr
ENST00000509205.5:c.*230G>C	ENSP00000427109.1:n.*230G>C
NM_001046.2:c.3617G>C	NP_001037.1:p.Ser1206Thr
NM_001256461.1:c.3569G>C	NP_001243390.1:p.Ser1190Thr
NR_046207.1:n.3847G>C
XM_017009771.1:c.1859G>C	XP_016865260.1:p.Ser620Thr
XR_001742214.1:n.3841G>C
NM_001046.3:c.3617G>C MANE Select	NP_001037.1:p.Ser1206Thr
NM_001256461.2:c.3569G>C	NP_001243390.1:p.Ser1190Thr
NR_046207.2:n.3872G>C