Canonical Allele Identifier: CA409271704

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1323271310
• gnomAD v3: 20-46726876-T-C
• gnomAD v4: 20-46726876-T-C
• MyVariant Identifiers: chr20:g.45355515T>C (hg19) ; chr20:g.46726876T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726876T>C , CM000682.2:g.46726876T>C	GRCh38
NC_000020.10:g.45355515T>C , CM000682.1:g.45355515T>C	GRCh37
NC_000020.9:g.44788922T>C	NCBI36
NG_016284.1:g.22237T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1301T>C MANE Select	ENSP00000352216.2:p.Val434Ala
ENST00000359271.3:c.1301T>C	ENSP00000352216.2:p.Val434Ala
NM_030777.3:c.1301T>C	NP_110404.1:p.Val434Ala
XM_011529060.1:c.1364T>C	XP_011527362.1:p.Val455Ala
XM_011529061.1:c.1310T>C	XP_011527363.1:p.Val437Ala
XM_011529062.1:c.1413T>C	XP_011527364.1:p.Cys471=
XM_011529063.1:c.1364T>C	XP_011527365.1:p.Val455Ala
XM_011529064.1:c.1413T>C	XP_011527366.1:p.Cys471=
XM_011529065.1:c.1364T>C	XP_011527367.1:p.Val455Ala
XR_936641.1:n.1549T>C
XM_011529060.2:c.1364T>C	XP_011527362.1:p.Val455Ala
XM_011529061.2:c.1310T>C	XP_011527363.1:p.Val437Ala
XM_011529062.2:c.1413T>C	XP_011527364.1:p.Cys471=
XM_011529063.2:c.1364T>C	XP_011527365.1:p.Val455Ala
XM_011529064.2:c.1413T>C	XP_011527366.1:p.Cys471=
XM_011529065.2:c.1364T>C	XP_011527367.1:p.Val455Ala
XM_017028087.2:c.1301T>C	XP_016883576.1:p.Val434Ala
XR_936641.2:n.1536T>C
NM_030777.4:c.1301T>C MANE Select	NP_110404.1:p.Val434Ala