Canonical Allele Identifier: CA2841658304

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725764_46725766del , CM000682.2:g.46725764_46725766del	GRCh38
NC_000020.10:g.45354403_45354405del , CM000682.1:g.45354403_45354405del	GRCh37
NC_000020.9:g.44787810_44787812del	NCBI36
NG_016284.1:g.21125_21127del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.728_730del MANE Select	ENSP00000352216.2:p.Gln243del
ENST00000359271.3:c.728_730del	ENSP00000352216.2:p.Gln243del
NM_030777.3:c.728_730del	NP_110404.1:p.Gln243del
XM_011529060.1:c.791_793del	XP_011527362.1:p.Gln264del
XM_011529061.1:c.737_739del	XP_011527363.1:p.Gln246del
XM_011529062.1:c.791_793del	XP_011527364.1:p.Gln264del
XM_011529063.1:c.791_793del	XP_011527365.1:p.Gln264del
XM_011529064.1:c.791_793del	XP_011527366.1:p.Gln264del
XM_011529065.1:c.791_793del	XP_011527367.1:p.Gln264del
XR_936641.1:n.927_929del
XM_011529060.2:c.791_793del	XP_011527362.1:p.Gln264del
XM_011529061.2:c.737_739del	XP_011527363.1:p.Gln246del
XM_011529062.2:c.791_793del	XP_011527364.1:p.Gln264del
XM_011529063.2:c.791_793del	XP_011527365.1:p.Gln264del
XM_011529064.2:c.791_793del	XP_011527366.1:p.Gln264del
XM_011529065.2:c.791_793del	XP_011527367.1:p.Gln264del
XM_017028087.2:c.728_730del	XP_016883576.1:p.Gln243del
XR_936641.2:n.914_916del
NM_030777.4:c.728_730del MANE Select	NP_110404.1:p.Gln243del