Canonical Allele Identifier: CA2573050850
Gene: ADAMTS13 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436853_133436874del , CM000671.2:g.133436853_133436874del GRCh38
NC_000009.10:g.135291794_135291815del NCBI36
NG_011934.2:g.27515_27536del , LRG_544:g.27515_27536del

Transcript Alleles

HGVS Amino-acid change
ENST00000355699.7:c.1333_1354del MANE Select ENSP00000347927.2:p.Phe445GlyfsTer?
ENST00000355699.6:c.1333_1354del ENSP00000347927.2:p.Phe445GlyfsTer?
ENST00000356589.6:c.1240_1261del ENSP00000348997.2:p.Phe414GlyfsTer?
ENST00000371916.5:c.589_610del ENSP00000360984.2:p.Phe197GlyfsTer?
ENST00000371929.7:c.1333_1354del ENSP00000360997.3:p.Phe445GlyfsTer?
ENST00000474918.1:c.*137_*158del ENSP00000435305.1:n.*137_*158del
ENST00000485925.5:n.974-2513_974-2492del
ENST00000495234.5:c.*617_*638del ENSP00000435274.1:n.*617_*638del
NM_139025.4:c.1333_1354del , LRG_544t1:c.1333_1354del NP_620594.1:p.Phe445GlyfsTer?
NM_139026.4:c.1240_1261del NP_620595.1:p.Phe414GlyfsTer?
NM_139027.4:c.1333_1354del NP_620596.2:p.Phe445GlyfsTer?
NR_024514.2:n.993-2513_993-2492del
XM_011518174.1:c.943_964del XP_011516476.1:p.Phe315GlyfsTer?
XM_011518175.1:c.1333_1354del XP_011516477.1:p.Phe445GlyfsTer?
XM_011518176.1:c.349_370del XP_011516478.1:p.Phe117GlyfsTer?
XM_011518177.1:c.343_364del XP_011516479.1:p.Phe115GlyfsTer?
XM_011518178.1:c.-3_19del
XM_011518179.1:c.119_140del XP_011516481.1:p.Val40GlyfsTer?
XM_011518180.1:c.687-8010_687-7989del XP_011516482.1:n.687-8010_687-7989del
XM_011518176.3:c.349_370del XP_011516478.1:p.Phe117GlyfsTer?
XM_011518178.2:c.-3_19del
XM_017014232.1:c.1321_1342del XP_016869721.1:p.Phe441GlyfsTer?
XM_017014233.1:c.943_964del XP_016869722.1:p.Phe315GlyfsTer?
XM_017014234.2:c.343_364del XP_016869723.1:p.Phe115GlyfsTer?
XM_017014235.1:c.1333_1354del XP_016869724.1:p.Phe445GlyfsTer?
XR_001746171.1:n.2558_2579del
NM_139026.5:c.1240_1261del NP_620595.1:p.Phe414GlyfsTer?
NM_139027.5:c.1333_1354del NP_620596.2:p.Phe445GlyfsTer?
NM_139025.5:c.1333_1354del NP_620594.1:p.Phe445GlyfsTer?
NM_139026.6:c.1240_1261del NP_620595.1:p.Phe414GlyfsTer?
NM_139027.6:c.1333_1354del MANE Select NP_620596.2:p.Phe445GlyfsTer?
NR_024514.3:n.995-2513_995-2492del