Canonical Allele Identifier: CA1017977506

Gene: SLC2A10

Linked Data

• gnomAD v3: 20-46726861-T-TTTTG
• gnomAD v4: 20-46726861-T-TTTTG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46726861_46726862insTTTG , CM000682.2:g.46726861_46726862insTTTG	GRCh38
NC_000020.10:g.45355500_45355501insTTTG , CM000682.1:g.45355500_45355501insTTTG	GRCh37
NC_000020.9:g.44788907_44788908insTTTG	NCBI36
NG_016284.1:g.22222_22223insTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1289-3_1289-2insTTTG MANE Select	ENSP00000352216.2:n.1289-3_1289-2insTTTG
ENST00000359271.3:c.1289-3_1289-2insTTTG	ENSP00000352216.2:n.1289-3_1289-2insTTTG
NM_030777.3:c.1289-3_1289-2insTTTG	NP_110404.1:n.1289-3_1289-2insTTTG
XM_011529060.1:c.1352-3_1352-2insTTTG	XP_011527362.1:n.1352-3_1352-2insTTTG
XM_011529061.1:c.1298-3_1298-2insTTTG	XP_011527363.1:n.1298-3_1298-2insTTTG
XM_011529062.1:c.1398_1399insTTTG	XP_011527364.1:p.Ser467PhefsTer3
XM_011529063.1:c.1352-3_1352-2insTTTG	XP_011527365.1:n.1352-3_1352-2insTTTG
XM_011529064.1:c.1398_1399insTTTG	XP_011527366.1:p.Ser467PhefsTer3
XM_011529065.1:c.1352-3_1352-2insTTTG	XP_011527367.1:n.1352-3_1352-2insTTTG
XR_936641.1:n.1534_1535insTTTG
XM_011529060.2:c.1352-3_1352-2insTTTG	XP_011527362.1:n.1352-3_1352-2insTTTG
XM_011529061.2:c.1298-3_1298-2insTTTG	XP_011527363.1:n.1298-3_1298-2insTTTG
XM_011529062.2:c.1398_1399insTTTG	XP_011527364.1:p.Ser467PhefsTer3
XM_011529063.2:c.1352-3_1352-2insTTTG	XP_011527365.1:n.1352-3_1352-2insTTTG
XM_011529064.2:c.1398_1399insTTTG	XP_011527366.1:p.Ser467PhefsTer3
XM_011529065.2:c.1352-3_1352-2insTTTG	XP_011527367.1:n.1352-3_1352-2insTTTG
XM_017028087.2:c.1289-3_1289-2insTTTG	XP_016883576.1:n.1289-3_1289-2insTTTG
XR_936641.2:n.1521_1522insTTTG
NM_030777.4:c.1289-3_1289-2insTTTG MANE Select	NP_110404.1:n.1289-3_1289-2insTTTG