Canonical Allele Identifier: CA510847838

Gene: SLC2A10

Linked Data

• MyVariant Identifiers: chr20:g.45354386G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725747G>T , CM000682.2:g.46725747G>T	GRCh38
NC_000020.10:g.45354386G>T , CM000682.1:g.45354386G>T	GRCh37
NC_000020.9:g.44787793G>T	NCBI36
NG_016284.1:g.21108G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.711G>T MANE Select	ENSP00000352216.2:p.Gly237=
ENST00000359271.3:c.711G>T	ENSP00000352216.2:p.Gly237=
NM_030777.3:c.711G>T	NP_110404.1:p.Gly237=
XM_011529060.1:c.774G>T	XP_011527362.1:p.Gly258=
XM_011529061.1:c.720G>T	XP_011527363.1:p.Gly240=
XM_011529062.1:c.774G>T	XP_011527364.1:p.Gly258=
XM_011529063.1:c.774G>T	XP_011527365.1:p.Gly258=
XM_011529064.1:c.774G>T	XP_011527366.1:p.Gly258=
XM_011529065.1:c.774G>T	XP_011527367.1:p.Gly258=
XR_936641.1:n.910G>T
XM_011529060.2:c.774G>T	XP_011527362.1:p.Gly258=
XM_011529061.2:c.720G>T	XP_011527363.1:p.Gly240=
XM_011529062.2:c.774G>T	XP_011527364.1:p.Gly258=
XM_011529063.2:c.774G>T	XP_011527365.1:p.Gly258=
XM_011529064.2:c.774G>T	XP_011527366.1:p.Gly258=
XM_011529065.2:c.774G>T	XP_011527367.1:p.Gly258=
XM_017028087.2:c.711G>T	XP_016883576.1:p.Gly237=
XR_936641.2:n.897G>T
NM_030777.4:c.711G>T MANE Select	NP_110404.1:p.Gly237=