Canonical Allele Identifier: CA2653171984
Gene: SLC2A10 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.46726913del , CM000682.2:g.46726913del GRCh38
NC_000020.10:g.45355552del , CM000682.1:g.45355552del GRCh37
NC_000020.9:g.44788959del NCBI36
NG_016284.1:g.22274del

Transcript Alleles

HGVS Amino-acid Change
ENST00000359271.4:c.1338del MANE Select ENSP00000352216.2:p.Ala447ProfsTer?
ENST00000359271.3:c.1338del ENSP00000352216.2:p.Ala447ProfsTer?
NM_030777.3:c.1338del NP_110404.1:p.Ala447ProfsTer?
XM_011529060.1:c.1401del XP_011527362.1:p.Ala468ProfsTer?
XM_011529061.1:c.1347del XP_011527363.1:p.Ala450ProfsTer?
XM_011529062.1:c.1450del XP_011527364.1:p.Ser484AlafsTer28
XM_011529063.1:c.1401del XP_011527365.1:p.Ala468ProfsTer?
XM_011529064.1:c.1450del XP_011527366.1:p.Ser484AlafsTer?
XM_011529065.1:c.1401del XP_011527367.1:p.Ala468ProfsTer?
XR_936641.1:n.1586del
XM_011529060.2:c.1401del XP_011527362.1:p.Ala468ProfsTer?
XM_011529061.2:c.1347del XP_011527363.1:p.Ala450ProfsTer?
XM_011529062.2:c.1450del XP_011527364.1:p.Ser484AlafsTer28
XM_011529063.2:c.1401del XP_011527365.1:p.Ala468ProfsTer?
XM_011529064.2:c.1450del XP_011527366.1:p.Ser484AlafsTer?
XM_011529065.2:c.1401del XP_011527367.1:p.Ala468ProfsTer?
XM_017028087.2:c.1338del XP_016883576.1:p.Ala447ProfsTer?
XR_936641.2:n.1573del
NM_030777.4:c.1338del MANE Select NP_110404.1:p.Ala447ProfsTer?