Canonical Allele Identifier: CA1017977493
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726859_46726860del , CM000682.2:g.46726859_46726860del GRCh38
NC_000020.10:g.45355498_45355499del , CM000682.1:g.45355498_45355499del GRCh37
NC_000020.9:g.44788905_44788906del NCBI36
NG_016284.1:g.22220_22221del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1289-5_1289-4del MANE Select ENSP00000352216.2:n.1289-5_1289-4del
ENST00000359271.3:c.1289-5_1289-4del ENSP00000352216.2:n.1289-5_1289-4del
NM_030777.3:c.1289-5_1289-4del NP_110404.1:n.1289-5_1289-4del
XM_011529060.1:c.1352-5_1352-4del XP_011527362.1:n.1352-5_1352-4del
XM_011529061.1:c.1298-5_1298-4del XP_011527363.1:n.1298-5_1298-4del
XM_011529062.1:c.1396_1397del XP_011527364.1:p.Pro466Ter
XM_011529063.1:c.1352-5_1352-4del XP_011527365.1:n.1352-5_1352-4del
XM_011529064.1:c.1396_1397del XP_011527366.1:p.Pro466Ter
XM_011529065.1:c.1352-5_1352-4del XP_011527367.1:n.1352-5_1352-4del
XR_936641.1:n.1532_1533del
XM_011529060.2:c.1352-5_1352-4del XP_011527362.1:n.1352-5_1352-4del
XM_011529061.2:c.1298-5_1298-4del XP_011527363.1:n.1298-5_1298-4del
XM_011529062.2:c.1396_1397del XP_011527364.1:p.Pro466Ter
XM_011529063.2:c.1352-5_1352-4del XP_011527365.1:n.1352-5_1352-4del
XM_011529064.2:c.1396_1397del XP_011527366.1:p.Pro466Ter
XM_011529065.2:c.1352-5_1352-4del XP_011527367.1:n.1352-5_1352-4del
XM_017028087.2:c.1289-5_1289-4del XP_016883576.1:n.1289-5_1289-4del
XR_936641.2:n.1519_1520del
NM_030777.4:c.1289-5_1289-4del MANE Select NP_110404.1:n.1289-5_1289-4del