Canonical Allele Identifier: CA9892151

Gene: SLC2A10

Linked Data

• dbSNP Id: rs758355727
• ExAC: 20:45355462 TC / T
• gnomAD v2: 20-45355462-TC-T
• gnomAD v4: 20-46726823-TC-T
• MyVariant Identifiers: chr20:g.45355463del (hg19) ; chr20:g.46726824del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726826del , CM000682.2:g.46726826del	GRCh38
NC_000020.10:g.45355465del , CM000682.1:g.45355465del	GRCh37
NC_000020.9:g.44788872del	NCBI36
NG_016284.1:g.22187del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-38del MANE Select	ENSP00000352216.2:n.1289-38del
ENST00000359271.3:c.1289-38del	ENSP00000352216.2:n.1289-38del
NM_030777.3:c.1289-38del	NP_110404.1:n.1289-38del
XM_011529060.1:c.1352-38del	XP_011527362.1:n.1352-38del
XM_011529061.1:c.1298-38del	XP_011527363.1:n.1298-38del
XM_011529062.1:c.1363del	XP_011527364.1:p.His455ThrfsTer?
XM_011529063.1:c.1352-38del	XP_011527365.1:n.1352-38del
XM_011529064.1:c.1363del	XP_011527366.1:p.His455ThrfsTer?
XM_011529065.1:c.1352-38del	XP_011527367.1:n.1352-38del
XR_936641.1:n.1499del
XM_011529060.2:c.1352-38del	XP_011527362.1:n.1352-38del
XM_011529061.2:c.1298-38del	XP_011527363.1:n.1298-38del
XM_011529062.2:c.1363del	XP_011527364.1:p.His455ThrfsTer?
XM_011529063.2:c.1352-38del	XP_011527365.1:n.1352-38del
XM_011529064.2:c.1363del	XP_011527366.1:p.His455ThrfsTer?
XM_011529065.2:c.1352-38del	XP_011527367.1:n.1352-38del
XM_017028087.2:c.1289-38del	XP_016883576.1:n.1289-38del
XR_936641.2:n.1486del
NM_030777.4:c.1289-38del MANE Select	NP_110404.1:n.1289-38del