Canonical Allele Identifier: CA2366796857

Gene: SLC2A10

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726823_46726824delinsTC , CM000682.2:g.46726823_46726824delinsTC	GRCh38
NC_000020.10:g.45355462_45355463delinsTC , CM000682.1:g.45355462_45355463delinsTC	GRCh37
NC_000020.9:g.44788869_44788870delinsTC	NCBI36
NG_016284.1:g.22184_22185delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-41_1289-40delinsTC MANE Select	ENSP00000352216.2:n.1289-41_1289-40delinsTC
ENST00000359271.3:c.1289-41_1289-40delinsTC	ENSP00000352216.2:n.1289-41_1289-40delinsTC
NM_030777.3:c.1289-41_1289-40delinsTC	NP_110404.1:n.1289-41_1289-40delinsTC
XM_011529060.1:c.1352-41_1352-40delinsTC	XP_011527362.1:n.1352-41_1352-40delinsTC
XM_011529061.1:c.1298-41_1298-40delinsTC	XP_011527363.1:n.1298-41_1298-40delinsTC
XM_011529062.1:c.1360_1361delinsTC	XP_011527364.1:p.Ser454=
XM_011529063.1:c.1352-41_1352-40delinsTC	XP_011527365.1:n.1352-41_1352-40delinsTC
XM_011529064.1:c.1360_1361delinsTC	XP_011527366.1:p.Ser454=
XM_011529065.1:c.1352-41_1352-40delinsTC	XP_011527367.1:n.1352-41_1352-40delinsTC
XR_936641.1:n.1496_1497delinsTC
XM_011529060.2:c.1352-41_1352-40delinsTC	XP_011527362.1:n.1352-41_1352-40delinsTC
XM_011529061.2:c.1298-41_1298-40delinsTC	XP_011527363.1:n.1298-41_1298-40delinsTC
XM_011529062.2:c.1360_1361delinsTC	XP_011527364.1:p.Ser454=
XM_011529063.2:c.1352-41_1352-40delinsTC	XP_011527365.1:n.1352-41_1352-40delinsTC
XM_011529064.2:c.1360_1361delinsTC	XP_011527366.1:p.Ser454=
XM_011529065.2:c.1352-41_1352-40delinsTC	XP_011527367.1:n.1352-41_1352-40delinsTC
XM_017028087.2:c.1289-41_1289-40delinsTC	XP_016883576.1:n.1289-41_1289-40delinsTC
XR_936641.2:n.1483_1484delinsTC
NM_030777.4:c.1289-41_1289-40delinsTC MANE Select	NP_110404.1:n.1289-41_1289-40delinsTC