Canonical Allele Identifier: CA2692370907
Gene: ADAMTS13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436830_133436906del , CM000671.2:g.133436830_133436906del GRCh38
NC_000009.10:g.135291771_135291847del NCBI36
NG_011934.2:g.27492_27568del , LRG_544:g.27492_27568del

Transcript Alleles

HGVS Amino-acid change
ENST00000355699.7:c.1310_1386del MANE Select ENSP00000347927.2:p.Ala437GlyfsTer?
ENST00000355699.6:c.1310_1386del ENSP00000347927.2:p.Ala437GlyfsTer?
ENST00000356589.6:c.1217_1293del ENSP00000348997.2:p.Ala406GlyfsTer?
ENST00000371916.5:c.566_642del ENSP00000360984.2:p.Ala189GlyfsTer?
ENST00000371929.7:c.1310_1386del ENSP00000360997.3:p.Ala437GlyfsTer?
ENST00000474918.1:c.*114_*190del ENSP00000435305.1:n.*114_*190del
ENST00000485925.5:n.974-2536_974-2460del
ENST00000495234.5:c.*594_*670del ENSP00000435274.1:n.*594_*670del
NM_139025.4:c.1310_1386del , LRG_544t1:c.1310_1386del NP_620594.1:p.Ala437GlyfsTer?
NM_139026.4:c.1217_1293del NP_620595.1:p.Ala406GlyfsTer?
NM_139027.4:c.1310_1386del NP_620596.2:p.Ala437GlyfsTer?
NR_024514.2:n.993-2536_993-2460del
XM_011518174.1:c.920_996del XP_011516476.1:p.Ala307GlyfsTer?
XM_011518175.1:c.1310_1386del XP_011516477.1:p.Ala437GlyfsTer?
XM_011518176.1:c.326_402del XP_011516478.1:p.Ala109GlyfsTer?
XM_011518177.1:c.320_396del XP_011516479.1:p.Ala107GlyfsTer?
XM_011518178.1:c.-26_51del
XM_011518179.1:c.96_172del XP_011516481.1:p.Leu33AlafsTer?
XM_011518180.1:c.687-8033_687-7957del XP_011516482.1:n.687-8033_687-7957del
XM_011518176.3:c.326_402del XP_011516478.1:p.Ala109GlyfsTer?
XM_011518178.2:c.-26_51del
XM_017014232.1:c.1298_1374del XP_016869721.1:p.Ala433GlyfsTer?
XM_017014233.1:c.920_996del XP_016869722.1:p.Ala307GlyfsTer?
XM_017014234.2:c.320_396del XP_016869723.1:p.Ala107GlyfsTer?
XM_017014235.1:c.1310_1386del XP_016869724.1:p.Ala437GlyfsTer?
XR_001746171.1:n.2535_2611del
NM_139026.5:c.1217_1293del NP_620595.1:p.Ala406GlyfsTer?
NM_139027.5:c.1310_1386del NP_620596.2:p.Ala437GlyfsTer?
NM_139025.5:c.1310_1386del NP_620594.1:p.Ala437GlyfsTer?
NM_139026.6:c.1217_1293del NP_620595.1:p.Ala406GlyfsTer?
NM_139027.6:c.1310_1386del MANE Select NP_620596.2:p.Ala437GlyfsTer?
NR_024514.3:n.995-2536_995-2460del