Canonical Allele Identifier: CA2366796242

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725519_46725520delinsCT , CM000682.2:g.46725519_46725520delinsCT	GRCh38
NC_000020.10:g.45354158_45354159delinsCT , CM000682.1:g.45354158_45354159delinsCT	GRCh37
NC_000020.9:g.44787565_44787566delinsCT	NCBI36
NG_016284.1:g.20880_20881delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.483_484delinsCT MANE Select	ENSP00000352216.2:p.Pro161=
ENST00000359271.3:c.483_484delinsCT	ENSP00000352216.2:p.Pro161=
NM_030777.3:c.483_484delinsCT	NP_110404.1:p.Pro161=
XM_011529060.1:c.546_547delinsCT	XP_011527362.1:p.Pro182=
XM_011529061.1:c.492_493delinsCT	XP_011527363.1:p.Pro164=
XM_011529062.1:c.546_547delinsCT	XP_011527364.1:p.Pro182=
XM_011529063.1:c.546_547delinsCT	XP_011527365.1:p.Pro182=
XM_011529064.1:c.546_547delinsCT	XP_011527366.1:p.Pro182=
XM_011529065.1:c.546_547delinsCT	XP_011527367.1:p.Pro182=
XR_936641.1:n.682_683delinsCT
XM_011529060.2:c.546_547delinsCT	XP_011527362.1:p.Pro182=
XM_011529061.2:c.492_493delinsCT	XP_011527363.1:p.Pro164=
XM_011529062.2:c.546_547delinsCT	XP_011527364.1:p.Pro182=
XM_011529063.2:c.546_547delinsCT	XP_011527365.1:p.Pro182=
XM_011529064.2:c.546_547delinsCT	XP_011527366.1:p.Pro182=
XM_011529065.2:c.546_547delinsCT	XP_011527367.1:p.Pro182=
XM_017028087.2:c.483_484delinsCT	XP_016883576.1:p.Pro161=
XR_936641.2:n.669_670delinsCT
NM_030777.4:c.483_484delinsCT MANE Select	NP_110404.1:p.Pro161=