Canonical Allele Identifier: CA2366796906

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726907_46726908delinsAG , CM000682.2:g.46726907_46726908delinsAG	GRCh38
NC_000020.10:g.45355546_45355547delinsAG , CM000682.1:g.45355546_45355547delinsAG	GRCh37
NC_000020.9:g.44788953_44788954delinsAG	NCBI36
NG_016284.1:g.22268_22269delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1332_1333delinsAG MANE Select	ENSP00000352216.2:p.Arg444=
ENST00000359271.3:c.1332_1333delinsAG	ENSP00000352216.2:p.Arg444=
NM_030777.3:c.1332_1333delinsAG	NP_110404.1:p.Arg444=
XM_011529060.1:c.1395_1396delinsAG	XP_011527362.1:p.Arg465=
XM_011529061.1:c.1341_1342delinsAG	XP_011527363.1:p.Arg447=
XM_011529062.1:c.1444_1445delinsAG	XP_011527364.1:p.Arg482=
XM_011529063.1:c.1395_1396delinsAG	XP_011527365.1:p.Arg465=
XM_011529064.1:c.1444_1445delinsAG	XP_011527366.1:p.Arg482=
XM_011529065.1:c.1395_1396delinsAG	XP_011527367.1:p.Arg465=
XR_936641.1:n.1580_1581delinsAG
XM_011529060.2:c.1395_1396delinsAG	XP_011527362.1:p.Arg465=
XM_011529061.2:c.1341_1342delinsAG	XP_011527363.1:p.Arg447=
XM_011529062.2:c.1444_1445delinsAG	XP_011527364.1:p.Arg482=
XM_011529063.2:c.1395_1396delinsAG	XP_011527365.1:p.Arg465=
XM_011529064.2:c.1444_1445delinsAG	XP_011527366.1:p.Arg482=
XM_011529065.2:c.1395_1396delinsAG	XP_011527367.1:p.Arg465=
XM_017028087.2:c.1332_1333delinsAG	XP_016883576.1:p.Arg444=
XR_936641.2:n.1567_1568delinsAG
NM_030777.4:c.1332_1333delinsAG MANE Select	NP_110404.1:p.Arg444=