Canonical Allele Identifier: CA2366796887

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726872_46726874delinsCTT , CM000682.2:g.46726872_46726874delinsCTT	GRCh38
NC_000020.10:g.45355511_45355513delinsCTT , CM000682.1:g.45355511_45355513delinsCTT	GRCh37
NC_000020.9:g.44788918_44788920delinsCTT	NCBI36
NG_016284.1:g.22233_22235delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1297_1299delinsCTT MANE Select	ENSP00000352216.2:p.Leu433=
ENST00000359271.3:c.1297_1299delinsCTT	ENSP00000352216.2:p.Leu433=
NM_030777.3:c.1297_1299delinsCTT	NP_110404.1:p.Leu433=
XM_011529060.1:c.1360_1362delinsCTT	XP_011527362.1:p.Leu454=
XM_011529061.1:c.1306_1308delinsCTT	XP_011527363.1:p.Leu436=
XM_011529062.1:c.1409_1411delinsCTT	XP_011527364.1:p.Ala470=
XM_011529063.1:c.1360_1362delinsCTT	XP_011527365.1:p.Leu454=
XM_011529064.1:c.1409_1411delinsCTT	XP_011527366.1:p.Ala470=
XM_011529065.1:c.1360_1362delinsCTT	XP_011527367.1:p.Leu454=
XR_936641.1:n.1545_1547delinsCTT
XM_011529060.2:c.1360_1362delinsCTT	XP_011527362.1:p.Leu454=
XM_011529061.2:c.1306_1308delinsCTT	XP_011527363.1:p.Leu436=
XM_011529062.2:c.1409_1411delinsCTT	XP_011527364.1:p.Ala470=
XM_011529063.2:c.1360_1362delinsCTT	XP_011527365.1:p.Leu454=
XM_011529064.2:c.1409_1411delinsCTT	XP_011527366.1:p.Ala470=
XM_011529065.2:c.1360_1362delinsCTT	XP_011527367.1:p.Leu454=
XM_017028087.2:c.1297_1299delinsCTT	XP_016883576.1:p.Leu433=
XR_936641.2:n.1532_1534delinsCTT
NM_030777.4:c.1297_1299delinsCTT MANE Select	NP_110404.1:p.Leu433=