Canonical Allele Identifier: CA510847824

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 2079423
• ClinVar RCV Id: RCV002995363
• gnomAD v4: 20-46725735-A-G
• MyVariant Identifiers: chr20:g.45354374A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725735A>G , CM000682.2:g.46725735A>G	GRCh38
NC_000020.10:g.45354374A>G , CM000682.1:g.45354374A>G	GRCh37
NC_000020.9:g.44787781A>G	NCBI36
NG_016284.1:g.21096A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.699A>G MANE Select	ENSP00000352216.2:p.Thr233=
ENST00000359271.3:c.699A>G	ENSP00000352216.2:p.Thr233=
NM_030777.3:c.699A>G	NP_110404.1:p.Thr233=
XM_011529060.1:c.762A>G	XP_011527362.1:p.Thr254=
XM_011529061.1:c.708A>G	XP_011527363.1:p.Thr236=
XM_011529062.1:c.762A>G	XP_011527364.1:p.Thr254=
XM_011529063.1:c.762A>G	XP_011527365.1:p.Thr254=
XM_011529064.1:c.762A>G	XP_011527366.1:p.Thr254=
XM_011529065.1:c.762A>G	XP_011527367.1:p.Thr254=
XR_936641.1:n.898A>G
XM_011529060.2:c.762A>G	XP_011527362.1:p.Thr254=
XM_011529061.2:c.708A>G	XP_011527363.1:p.Thr236=
XM_011529062.2:c.762A>G	XP_011527364.1:p.Thr254=
XM_011529063.2:c.762A>G	XP_011527365.1:p.Thr254=
XM_011529064.2:c.762A>G	XP_011527366.1:p.Thr254=
XM_011529065.2:c.762A>G	XP_011527367.1:p.Thr254=
XM_017028087.2:c.699A>G	XP_016883576.1:p.Thr233=
XR_936641.2:n.885A>G
NM_030777.4:c.699A>G MANE Select	NP_110404.1:p.Thr233=