Canonical Allele Identifier: CA409266784

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45354000G>C (hg19) ; chr20:g.46725361G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725361G>C , CM000682.2:g.46725361G>C	GRCh38
NC_000020.10:g.45354000G>C , CM000682.1:g.45354000G>C	GRCh37
NC_000020.9:g.44787407G>C	NCBI36
NG_016284.1:g.20722G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.325G>C MANE Select	ENSP00000352216.2:p.Gly109Arg
ENST00000359271.3:c.325G>C	ENSP00000352216.2:p.Gly109Arg
ENST00000611837.1:n.477G>C
NM_030777.3:c.325G>C	NP_110404.1:p.Gly109Arg
XM_011529060.1:c.388G>C	XP_011527362.1:p.Gly130Arg
XM_011529061.1:c.334G>C	XP_011527363.1:p.Gly112Arg
XM_011529062.1:c.388G>C	XP_011527364.1:p.Gly130Arg
XM_011529063.1:c.388G>C	XP_011527365.1:p.Gly130Arg
XM_011529064.1:c.388G>C	XP_011527366.1:p.Gly130Arg
XM_011529065.1:c.388G>C	XP_011527367.1:p.Gly130Arg
XR_936641.1:n.524G>C
XM_011529060.2:c.388G>C	XP_011527362.1:p.Gly130Arg
XM_011529061.2:c.334G>C	XP_011527363.1:p.Gly112Arg
XM_011529062.2:c.388G>C	XP_011527364.1:p.Gly130Arg
XM_011529063.2:c.388G>C	XP_011527365.1:p.Gly130Arg
XM_011529064.2:c.388G>C	XP_011527366.1:p.Gly130Arg
XM_011529065.2:c.388G>C	XP_011527367.1:p.Gly130Arg
XM_017028087.2:c.325G>C	XP_016883576.1:p.Gly109Arg
XR_936641.2:n.511G>C
NM_030777.4:c.325G>C MANE Select	NP_110404.1:p.Gly109Arg