Canonical Allele Identifier: CA375391444
Gene: ADAMTS13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133436838A>T (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436838A>T , CM000671.2:g.133436838A>T GRCh38
NC_000009.10:g.135291779A>T NCBI36
NG_011934.2:g.27500A>T , LRG_544:g.27500A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355699.7:c.1318A>T MANE Select ENSP00000347927.2:p.Lys440Ter
ENST00000355699.6:c.1318A>T ENSP00000347927.2:p.Lys440Ter
ENST00000356589.6:c.1225A>T ENSP00000348997.2:p.Lys409Ter
ENST00000371916.5:c.574A>T ENSP00000360984.2:p.Lys192Ter
ENST00000371929.7:c.1318A>T ENSP00000360997.3:p.Lys440Ter
ENST00000474918.1:c.*122A>T ENSP00000435305.1:n.*122A>T
ENST00000485925.5:n.974-2528A>T
ENST00000495234.5:c.*602A>T ENSP00000435274.1:n.*602A>T
NM_139025.4:c.1318A>T , LRG_544t1:c.1318A>T NP_620594.1:p.Lys440Ter
NM_139026.4:c.1225A>T NP_620595.1:p.Lys409Ter
NM_139027.4:c.1318A>T NP_620596.2:p.Lys440Ter
NR_024514.2:n.993-2528A>T
XM_011518174.1:c.928A>T XP_011516476.1:p.Lys310Ter
XM_011518175.1:c.1318A>T XP_011516477.1:p.Lys440Ter
XM_011518176.1:c.334A>T XP_011516478.1:p.Lys112Ter
XM_011518177.1:c.328A>T XP_011516479.1:p.Lys110Ter
XM_011518178.1:c.-18A>T XP_011516480.1:n.-18A>T
XM_011518179.1:c.104A>T XP_011516481.1:p.Glu35Val
XM_011518180.1:c.687-8025A>T XP_011516482.1:n.687-8025A>T
XM_011518176.3:c.334A>T XP_011516478.1:p.Lys112Ter
XM_011518178.2:c.-18A>T XP_011516480.1:n.-18A>T
XM_017014232.1:c.1306A>T XP_016869721.1:p.Lys436Ter
XM_017014233.1:c.928A>T XP_016869722.1:p.Lys310Ter
XM_017014234.2:c.328A>T XP_016869723.1:p.Lys110Ter
XM_017014235.1:c.1318A>T XP_016869724.1:p.Lys440Ter
XR_001746171.1:n.2543A>T
NM_139026.5:c.1225A>T NP_620595.1:p.Lys409Ter
NM_139027.5:c.1318A>T NP_620596.2:p.Lys440Ter
NM_139025.5:c.1318A>T NP_620594.1:p.Lys440Ter
NM_139026.6:c.1225A>T NP_620595.1:p.Lys409Ter
NM_139027.6:c.1318A>T MANE Select NP_620596.2:p.Lys440Ter
NR_024514.3:n.995-2528A>T