Canonical Allele Identifier: CA510771318

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45355606C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726967C>G , CM000682.2:g.46726967C>G	GRCh38
NC_000020.10:g.45355606C>G , CM000682.1:g.45355606C>G	GRCh37
NC_000020.9:g.44789013C>G	NCBI36
NG_016284.1:g.22328C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.1392C>G MANE Select	ENSP00000352216.2:p.Leu464=
ENST00000359271.3:c.1392C>G	ENSP00000352216.2:p.Leu464=
NM_030777.3:c.1392C>G	NP_110404.1:p.Leu464=
XM_011529060.1:c.1455C>G	XP_011527362.1:p.Leu485=
XM_011529061.1:c.1401C>G	XP_011527363.1:p.Leu467=
XM_011529062.1:c.1504C>G	XP_011527364.1:p.Leu502Val
XM_011529063.1:c.1455C>G	XP_011527365.1:p.Leu485=
XM_011529064.1:c.1504C>G	XP_011527366.1:p.Leu502Val
XM_011529065.1:c.1455C>G	XP_011527367.1:p.Leu485=
XR_936641.1:n.1640C>G
XM_011529060.2:c.1455C>G	XP_011527362.1:p.Leu485=
XM_011529061.2:c.1401C>G	XP_011527363.1:p.Leu467=
XM_011529062.2:c.1504C>G	XP_011527364.1:p.Leu502Val
XM_011529063.2:c.1455C>G	XP_011527365.1:p.Leu485=
XM_011529064.2:c.1504C>G	XP_011527366.1:p.Leu502Val
XM_011529065.2:c.1455C>G	XP_011527367.1:p.Leu485=
XM_017028087.2:c.1392C>G	XP_016883576.1:p.Leu464=
XR_936641.2:n.1627C>G
NM_030777.4:c.1392C>G MANE Select	NP_110404.1:p.Leu464=