Canonical Allele Identifier: CA9891934

Gene: SLC2A10

Linked Data

• dbSNP Id: rs369865870
• ExAC: 20:45353913 G / T
• gnomAD v2: 20-45353913-G-T
• gnomAD v3: 20-46725274-G-T
• gnomAD v4: 20-46725274-G-T
• COSMIC: COSM6377997
• MyVariant Identifiers: chr20:g.45353913G>T (hg19) ; chr20:g.46725274G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725274G>T , CM000682.2:g.46725274G>T	GRCh38
NC_000020.10:g.45353913G>T , CM000682.1:g.45353913G>T	GRCh37
NC_000020.9:g.44787320G>T	NCBI36
NG_016284.1:g.20635G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000359271.4:c.238G>T MANE Select	ENSP00000352216.2:p.Gly80Trp
ENST00000359271.3:c.238G>T	ENSP00000352216.2:p.Gly80Trp
ENST00000611837.1:n.390G>T
NM_030777.3:c.238G>T	NP_110404.1:p.Gly80Trp
XM_011529060.1:c.301G>T	XP_011527362.1:p.Gly101Trp
XM_011529061.1:c.247G>T	XP_011527363.1:p.Gly83Trp
XM_011529062.1:c.301G>T	XP_011527364.1:p.Gly101Trp
XM_011529063.1:c.301G>T	XP_011527365.1:p.Gly101Trp
XM_011529064.1:c.301G>T	XP_011527366.1:p.Gly101Trp
XM_011529065.1:c.301G>T	XP_011527367.1:p.Gly101Trp
XR_936641.1:n.437G>T
XM_011529060.2:c.301G>T	XP_011527362.1:p.Gly101Trp
XM_011529061.2:c.247G>T	XP_011527363.1:p.Gly83Trp
XM_011529062.2:c.301G>T	XP_011527364.1:p.Gly101Trp
XM_011529063.2:c.301G>T	XP_011527365.1:p.Gly101Trp
XM_011529064.2:c.301G>T	XP_011527366.1:p.Gly101Trp
XM_011529065.2:c.301G>T	XP_011527367.1:p.Gly101Trp
XM_017028087.2:c.238G>T	XP_016883576.1:p.Gly80Trp
XR_936641.2:n.424G>T
NM_030777.4:c.238G>T MANE Select	NP_110404.1:p.Gly80Trp