Canonical Allele Identifier: CA409267146

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46725542-G-T
• MyVariant Identifiers: chr20:g.45354181G>T (hg19) ; chr20:g.46725542G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725542G>T , CM000682.2:g.46725542G>T	GRCh38
NC_000020.10:g.45354181G>T , CM000682.1:g.45354181G>T	GRCh37
NC_000020.9:g.44787588G>T	NCBI36
NG_016284.1:g.20903G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.506G>T MANE Select	ENSP00000352216.2:p.Gly169Val
ENST00000359271.3:c.506G>T	ENSP00000352216.2:p.Gly169Val
NM_030777.3:c.506G>T	NP_110404.1:p.Gly169Val
XM_011529060.1:c.569G>T	XP_011527362.1:p.Gly190Val
XM_011529061.1:c.515G>T	XP_011527363.1:p.Gly172Val
XM_011529062.1:c.569G>T	XP_011527364.1:p.Gly190Val
XM_011529063.1:c.569G>T	XP_011527365.1:p.Gly190Val
XM_011529064.1:c.569G>T	XP_011527366.1:p.Gly190Val
XM_011529065.1:c.569G>T	XP_011527367.1:p.Gly190Val
XR_936641.1:n.705G>T
XM_011529060.2:c.569G>T	XP_011527362.1:p.Gly190Val
XM_011529061.2:c.515G>T	XP_011527363.1:p.Gly172Val
XM_011529062.2:c.569G>T	XP_011527364.1:p.Gly190Val
XM_011529063.2:c.569G>T	XP_011527365.1:p.Gly190Val
XM_011529064.2:c.569G>T	XP_011527366.1:p.Gly190Val
XM_011529065.2:c.569G>T	XP_011527367.1:p.Gly190Val
XM_017028087.2:c.506G>T	XP_016883576.1:p.Gly169Val
XR_936641.2:n.692G>T
NM_030777.4:c.506G>T MANE Select	NP_110404.1:p.Gly169Val