Canonical Allele Identifier: CA409267419

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 467818
• ClinVar RCV Id: RCV000544217
• dbSNP Id: rs1555887956
• MyVariant Identifiers: chr20:g.45354286G>A (hg19) ; chr20:g.46725647G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725647G>A , CM000682.2:g.46725647G>A	GRCh38
NC_000020.10:g.45354286G>A , CM000682.1:g.45354286G>A	GRCh37
NC_000020.9:g.44787693G>A	NCBI36
NG_016284.1:g.21008G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.611G>A MANE Select	ENSP00000352216.2:p.Gly204Asp
ENST00000359271.3:c.611G>A	ENSP00000352216.2:p.Gly204Asp
NM_030777.3:c.611G>A	NP_110404.1:p.Gly204Asp
XM_011529060.1:c.674G>A	XP_011527362.1:p.Gly225Asp
XM_011529061.1:c.620G>A	XP_011527363.1:p.Gly207Asp
XM_011529062.1:c.674G>A	XP_011527364.1:p.Gly225Asp
XM_011529063.1:c.674G>A	XP_011527365.1:p.Gly225Asp
XM_011529064.1:c.674G>A	XP_011527366.1:p.Gly225Asp
XM_011529065.1:c.674G>A	XP_011527367.1:p.Gly225Asp
XR_936641.1:n.810G>A
XM_011529060.2:c.674G>A	XP_011527362.1:p.Gly225Asp
XM_011529061.2:c.620G>A	XP_011527363.1:p.Gly207Asp
XM_011529062.2:c.674G>A	XP_011527364.1:p.Gly225Asp
XM_011529063.2:c.674G>A	XP_011527365.1:p.Gly225Asp
XM_011529064.2:c.674G>A	XP_011527366.1:p.Gly225Asp
XM_011529065.2:c.674G>A	XP_011527367.1:p.Gly225Asp
XM_017028087.2:c.611G>A	XP_016883576.1:p.Gly204Asp
XR_936641.2:n.797G>A
NM_030777.4:c.611G>A MANE Select	NP_110404.1:p.Gly204Asp