Canonical Allele Identifier: CA510771255

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45355504G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726865G>T , CM000682.2:g.46726865G>T	GRCh38
NC_000020.10:g.45355504G>T , CM000682.1:g.45355504G>T	GRCh37
NC_000020.9:g.44788911G>T	NCBI36
NG_016284.1:g.22226G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.1290G>T MANE Select	ENSP00000352216.2:p.Val430=
ENST00000359271.3:c.1290G>T	ENSP00000352216.2:p.Val430=
NM_030777.3:c.1290G>T	NP_110404.1:p.Val430=
XM_011529060.1:c.1353G>T	XP_011527362.1:p.Val451=
XM_011529061.1:c.1299G>T	XP_011527363.1:p.Val433=
XM_011529062.1:c.1402G>T	XP_011527364.1:p.Asp468Tyr
XM_011529063.1:c.1353G>T	XP_011527365.1:p.Val451=
XM_011529064.1:c.1402G>T	XP_011527366.1:p.Asp468Tyr
XM_011529065.1:c.1353G>T	XP_011527367.1:p.Val451=
XR_936641.1:n.1538G>T
XM_011529060.2:c.1353G>T	XP_011527362.1:p.Val451=
XM_011529061.2:c.1299G>T	XP_011527363.1:p.Val433=
XM_011529062.2:c.1402G>T	XP_011527364.1:p.Asp468Tyr
XM_011529063.2:c.1353G>T	XP_011527365.1:p.Val451=
XM_011529064.2:c.1402G>T	XP_011527366.1:p.Asp468Tyr
XM_011529065.2:c.1353G>T	XP_011527367.1:p.Val451=
XM_017028087.2:c.1290G>T	XP_016883576.1:p.Val430=
XR_936641.2:n.1525G>T
NM_030777.4:c.1290G>T MANE Select	NP_110404.1:p.Val430=