Canonical Allele Identifier: CA9892027

Gene: SLC2A10

Linked Data

• ClinVar Variation Id: 241607
• ClinVar RCV Id: RCV000234521 ; RCV001578214 ; RCV002365216
• dbSNP Id: rs138679634
• ExAC: 20:45354371 C / G
• gnomAD v2: 20-45354371-C-G
• gnomAD v3: 20-46725732-C-G
• gnomAD v4: 20-46725732-C-G
• MyVariant Identifiers: chr20:g.45354371C>G (hg19) ; chr20:g.46725732C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725732C>G , CM000682.2:g.46725732C>G	GRCh38
NC_000020.10:g.45354371C>G , CM000682.1:g.45354371C>G	GRCh37
NC_000020.9:g.44787778C>G	NCBI36
NG_016284.1:g.21093C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.696C>G MANE Select	ENSP00000352216.2:p.Thr232=
ENST00000359271.3:c.696C>G	ENSP00000352216.2:p.Thr232=
NM_030777.3:c.696C>G	NP_110404.1:p.Thr232=
XM_011529060.1:c.759C>G	XP_011527362.1:p.Thr253=
XM_011529061.1:c.705C>G	XP_011527363.1:p.Thr235=
XM_011529062.1:c.759C>G	XP_011527364.1:p.Thr253=
XM_011529063.1:c.759C>G	XP_011527365.1:p.Thr253=
XM_011529064.1:c.759C>G	XP_011527366.1:p.Thr253=
XM_011529065.1:c.759C>G	XP_011527367.1:p.Thr253=
XR_936641.1:n.895C>G
XM_011529060.2:c.759C>G	XP_011527362.1:p.Thr253=
XM_011529061.2:c.705C>G	XP_011527363.1:p.Thr235=
XM_011529062.2:c.759C>G	XP_011527364.1:p.Thr253=
XM_011529063.2:c.759C>G	XP_011527365.1:p.Thr253=
XM_011529064.2:c.759C>G	XP_011527366.1:p.Thr253=
XM_011529065.2:c.759C>G	XP_011527367.1:p.Thr253=
XM_017028087.2:c.696C>G	XP_016883576.1:p.Thr232=
XR_936641.2:n.882C>G
NM_030777.4:c.696C>G MANE Select	NP_110404.1:p.Thr232=