Canonical Allele Identifier: CA2653172053

Gene: SLC2A10

Linked Data

• gnomAD v4: 20-46727034-CCTACT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46727038_46727042del , CM000682.2:g.46727038_46727042del	GRCh38
NC_000020.10:g.45355677_45355681del , CM000682.1:g.45355677_45355681del	GRCh37
NC_000020.9:g.44789084_44789088del	NCBI36
NG_016284.1:g.22399_22403del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359271.4:c.1411+52_1411+56del MANE Select	ENSP00000352216.2:n.1411+52_1411+56del
ENST00000359271.3:c.1411+52_1411+56del	ENSP00000352216.2:n.1411+52_1411+56del
NM_030777.3:c.1411+52_1411+56del	NP_110404.1:n.1411+52_1411+56del
XM_011529060.1:c.1474+52_1474+56del	XP_011527362.1:n.1474+52_1474+56del
XM_011529061.1:c.1420+52_1420+56del	XP_011527363.1:n.1420+52_1420+56del
XM_011529062.1:c.1523+52_1523+56del	XP_011527364.1:n.1523+52_1523+56del
XM_011529063.1:c.1474+52_1474+56del	XP_011527365.1:n.1474+52_1474+56del
XM_011529064.1:c.1523+52_1523+56del	XP_011527366.1:n.1523+52_1523+56del
XM_011529065.1:c.1474+52_1474+56del	XP_011527367.1:n.1474+52_1474+56del
XR_936641.1:n.1659+52_1659+56del
XM_011529060.2:c.1474+52_1474+56del	XP_011527362.1:n.1474+52_1474+56del
XM_011529061.2:c.1420+52_1420+56del	XP_011527363.1:n.1420+52_1420+56del
XM_011529062.2:c.1523+52_1523+56del	XP_011527364.1:n.1523+52_1523+56del
XM_011529063.2:c.1474+52_1474+56del	XP_011527365.1:n.1474+52_1474+56del
XM_011529064.2:c.1523+52_1523+56del	XP_011527366.1:n.1523+52_1523+56del
XM_011529065.2:c.1474+52_1474+56del	XP_011527367.1:n.1474+52_1474+56del
XM_017028087.2:c.1411+52_1411+56del	XP_016883576.1:n.1411+52_1411+56del
XR_936641.2:n.1646+52_1646+56del
NM_030777.4:c.1411+52_1411+56del MANE Select	NP_110404.1:n.1411+52_1411+56del