Canonical Allele Identifier: CA2653170688

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46724928-T-TG

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46724930dup , CM000682.2:g.46724930dup	GRCh38
NC_000020.10:g.45353569dup , CM000682.1:g.45353569dup	GRCh37
NC_000020.9:g.44786976dup	NCBI36
NG_016284.1:g.20291dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.5-111dup MANE Select	ENSP00000352216.2:n.5-111dup
ENST00000359271.3:c.5-111dup	ENSP00000352216.2:n.5-111dup
ENST00000611837.1:n.157-111dup
NM_030777.3:c.5-111dup	NP_110404.1:n.5-111dup
XM_011529060.1:c.68-111dup	XP_011527362.1:n.68-111dup
XM_011529061.1:c.14-111dup	XP_011527363.1:n.14-111dup
XM_011529062.1:c.68-111dup	XP_011527364.1:n.68-111dup
XM_011529063.1:c.68-111dup	XP_011527365.1:n.68-111dup
XM_011529064.1:c.68-111dup	XP_011527366.1:n.68-111dup
XM_011529065.1:c.68-111dup	XP_011527367.1:n.68-111dup
XR_936641.1:n.204-111dup
XM_011529060.2:c.68-111dup	XP_011527362.1:n.68-111dup
XM_011529061.2:c.14-111dup	XP_011527363.1:n.14-111dup
XM_011529062.2:c.68-111dup	XP_011527364.1:n.68-111dup
XM_011529063.2:c.68-111dup	XP_011527365.1:n.68-111dup
XM_011529064.2:c.68-111dup	XP_011527366.1:n.68-111dup
XM_011529065.2:c.68-111dup	XP_011527367.1:n.68-111dup
XM_017028087.2:c.5-111dup	XP_016883576.1:n.5-111dup
XR_936641.2:n.191-111dup
NM_030777.4:c.5-111dup MANE Select	NP_110404.1:n.5-111dup