Canonical Allele Identifier: CA2366796347

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46725740_46725741delinsGC , CM000682.2:g.46725740_46725741delinsGC	GRCh38
NC_000020.10:g.45354379_45354380delinsGC , CM000682.1:g.45354379_45354380delinsGC	GRCh37
NC_000020.9:g.44787786_44787787delinsGC	NCBI36
NG_016284.1:g.21101_21102delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.704_705delinsGC MANE Select	ENSP00000352216.2:p.Gly235=
ENST00000359271.3:c.704_705delinsGC	ENSP00000352216.2:p.Gly235=
NM_030777.3:c.704_705delinsGC	NP_110404.1:p.Gly235=
XM_011529060.1:c.767_768delinsGC	XP_011527362.1:p.Gly256=
XM_011529061.1:c.713_714delinsGC	XP_011527363.1:p.Gly238=
XM_011529062.1:c.767_768delinsGC	XP_011527364.1:p.Gly256=
XM_011529063.1:c.767_768delinsGC	XP_011527365.1:p.Gly256=
XM_011529064.1:c.767_768delinsGC	XP_011527366.1:p.Gly256=
XM_011529065.1:c.767_768delinsGC	XP_011527367.1:p.Gly256=
XR_936641.1:n.903_904delinsGC
XM_011529060.2:c.767_768delinsGC	XP_011527362.1:p.Gly256=
XM_011529061.2:c.713_714delinsGC	XP_011527363.1:p.Gly238=
XM_011529062.2:c.767_768delinsGC	XP_011527364.1:p.Gly256=
XM_011529063.2:c.767_768delinsGC	XP_011527365.1:p.Gly256=
XM_011529064.2:c.767_768delinsGC	XP_011527366.1:p.Gly256=
XM_011529065.2:c.767_768delinsGC	XP_011527367.1:p.Gly256=
XM_017028087.2:c.704_705delinsGC	XP_016883576.1:p.Gly235=
XR_936641.2:n.890_891delinsGC
NM_030777.4:c.704_705delinsGC MANE Select	NP_110404.1:p.Gly235=