Canonical Allele Identifier: CA2653171903

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46726749-T-TTA

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726749_46726750insTA , CM000682.2:g.46726749_46726750insTA	GRCh38
NC_000020.10:g.45355388_45355389insTA , CM000682.1:g.45355388_45355389insTA	GRCh37
NC_000020.9:g.44788795_44788796insTA	NCBI36
NG_016284.1:g.22110_22111insTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-115_1289-114insTA MANE Select	ENSP00000352216.2:n.1289-115_1289-114insTA
ENST00000359271.3:c.1289-115_1289-114insTA	ENSP00000352216.2:n.1289-115_1289-114insTA
NM_030777.3:c.1289-115_1289-114insTA	NP_110404.1:n.1289-115_1289-114insTA
XM_011529060.1:c.1352-115_1352-114insTA	XP_011527362.1:n.1352-115_1352-114insTA
XM_011529061.1:c.1298-115_1298-114insTA	XP_011527363.1:n.1298-115_1298-114insTA
XM_011529062.1:c.1352-66_1352-65insTA	XP_011527364.1:n.1352-66_1352-65insTA
XM_011529063.1:c.1352-115_1352-114insTA	XP_011527365.1:n.1352-115_1352-114insTA
XM_011529064.1:c.1352-66_1352-65insTA	XP_011527366.1:n.1352-66_1352-65insTA
XM_011529065.1:c.1352-115_1352-114insTA	XP_011527367.1:n.1352-115_1352-114insTA
XR_936641.1:n.1488-66_1488-65insTA
XM_011529060.2:c.1352-115_1352-114insTA	XP_011527362.1:n.1352-115_1352-114insTA
XM_011529061.2:c.1298-115_1298-114insTA	XP_011527363.1:n.1298-115_1298-114insTA
XM_011529062.2:c.1352-66_1352-65insTA	XP_011527364.1:n.1352-66_1352-65insTA
XM_011529063.2:c.1352-115_1352-114insTA	XP_011527365.1:n.1352-115_1352-114insTA
XM_011529064.2:c.1352-66_1352-65insTA	XP_011527366.1:n.1352-66_1352-65insTA
XM_011529065.2:c.1352-115_1352-114insTA	XP_011527367.1:n.1352-115_1352-114insTA
XM_017028087.2:c.1289-115_1289-114insTA	XP_016883576.1:n.1289-115_1289-114insTA
XR_936641.2:n.1475-66_1475-65insTA
NM_030777.4:c.1289-115_1289-114insTA MANE Select	NP_110404.1:n.1289-115_1289-114insTA