Canonical Allele Identifier: CA2366796821

Gene: SLC2A10

Linked Data

• dbSNP Id: rs1979985750
• gnomAD v4: 20-46726737-GT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726738del , CM000682.2:g.46726738del	GRCh38
NC_000020.10:g.45355377del , CM000682.1:g.45355377del	GRCh37
NC_000020.9:g.44788784del	NCBI36
NG_016284.1:g.22099del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-126del MANE Select	ENSP00000352216.2:n.1289-126del
ENST00000359271.3:c.1289-126del	ENSP00000352216.2:n.1289-126del
NM_030777.3:c.1289-126del	NP_110404.1:n.1289-126del
XM_011529060.1:c.1352-126del	XP_011527362.1:n.1352-126del
XM_011529061.1:c.1298-126del	XP_011527363.1:n.1298-126del
XM_011529062.1:c.1352-77del	XP_011527364.1:n.1352-77del
XM_011529063.1:c.1352-126del	XP_011527365.1:n.1352-126del
XM_011529064.1:c.1352-77del	XP_011527366.1:n.1352-77del
XM_011529065.1:c.1352-126del	XP_011527367.1:n.1352-126del
XR_936641.1:n.1488-77del
XM_011529060.2:c.1352-126del	XP_011527362.1:n.1352-126del
XM_011529061.2:c.1298-126del	XP_011527363.1:n.1298-126del
XM_011529062.2:c.1352-77del	XP_011527364.1:n.1352-77del
XM_011529063.2:c.1352-126del	XP_011527365.1:n.1352-126del
XM_011529064.2:c.1352-77del	XP_011527366.1:n.1352-77del
XM_011529065.2:c.1352-126del	XP_011527367.1:n.1352-126del
XM_017028087.2:c.1289-126del	XP_016883576.1:n.1289-126del
XR_936641.2:n.1475-77del
NM_030777.4:c.1289-126del MANE Select	NP_110404.1:n.1289-126del