Canonical Allele Identifier: CA510847802

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 798494
• ClinVar RCV Id: RCV000982039
• dbSNP Id: rs768433086
• MyVariant Identifiers: chr20:g.45354338C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725699C>A , CM000682.2:g.46725699C>A	GRCh38
NC_000020.10:g.45354338C>A , CM000682.1:g.45354338C>A	GRCh37
NC_000020.9:g.44787745C>A	NCBI36
NG_016284.1:g.21060C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.663C>A MANE Select	ENSP00000352216.2:p.Leu221=
ENST00000359271.3:c.663C>A	ENSP00000352216.2:p.Leu221=
NM_030777.3:c.663C>A	NP_110404.1:p.Leu221=
XM_011529060.1:c.726C>A	XP_011527362.1:p.Leu242=
XM_011529061.1:c.672C>A	XP_011527363.1:p.Leu224=
XM_011529062.1:c.726C>A	XP_011527364.1:p.Leu242=
XM_011529063.1:c.726C>A	XP_011527365.1:p.Leu242=
XM_011529064.1:c.726C>A	XP_011527366.1:p.Leu242=
XM_011529065.1:c.726C>A	XP_011527367.1:p.Leu242=
XR_936641.1:n.862C>A
XM_011529060.2:c.726C>A	XP_011527362.1:p.Leu242=
XM_011529061.2:c.672C>A	XP_011527363.1:p.Leu224=
XM_011529062.2:c.726C>A	XP_011527364.1:p.Leu242=
XM_011529063.2:c.726C>A	XP_011527365.1:p.Leu242=
XM_011529064.2:c.726C>A	XP_011527366.1:p.Leu242=
XM_011529065.2:c.726C>A	XP_011527367.1:p.Leu242=
XM_017028087.2:c.663C>A	XP_016883576.1:p.Leu221=
XR_936641.2:n.849C>A
NM_030777.4:c.663C>A MANE Select	NP_110404.1:p.Leu221=