Canonical Allele Identifier: CA1882673132
Gene: ADAMTS13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436874A= , CM000671.2:g.133436874A= GRCh38
NC_000009.10:g.135291815A= NCBI36
NG_011934.2:g.27536A= , LRG_544:g.27536A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355699.7:c.1354A= MANE Select ENSP00000347927.2:p.Arg452=
ENST00000355699.6:c.1354A= ENSP00000347927.2:p.Arg452=
ENST00000356589.6:c.1261A= ENSP00000348997.2:p.Arg421=
ENST00000371916.5:c.610A= ENSP00000360984.2:p.Arg204=
ENST00000371929.7:c.1354A= ENSP00000360997.3:p.Arg452=
ENST00000474918.1:c.*158A= ENSP00000435305.1:n.*158A=
ENST00000485925.5:n.974-2492A=
ENST00000495234.5:c.*638A= ENSP00000435274.1:n.*638A=
NM_139025.4:c.1354A= , LRG_544t1:c.1354A= NP_620594.1:p.Arg452=
NM_139026.4:c.1261A= NP_620595.1:p.Arg421=
NM_139027.4:c.1354A= NP_620596.2:p.Arg452=
NR_024514.2:n.993-2492A=
XM_011518174.1:c.964A= XP_011516476.1:p.Arg322=
XM_011518175.1:c.1354A= XP_011516477.1:p.Arg452=
XM_011518176.1:c.370A= XP_011516478.1:p.Arg124=
XM_011518177.1:c.364A= XP_011516479.1:p.Arg122=
XM_011518178.1:c.19A= XP_011516480.1:p.Arg7=
XM_011518179.1:c.140A= XP_011516481.1:p.Gln47=
XM_011518180.1:c.687-7989A= XP_011516482.1:n.687-7989A=
XM_011518176.3:c.370A= XP_011516478.1:p.Arg124=
XM_011518178.2:c.19A= XP_011516480.1:p.Arg7=
XM_017014232.1:c.1342A= XP_016869721.1:p.Arg448=
XM_017014233.1:c.964A= XP_016869722.1:p.Arg322=
XM_017014234.2:c.364A= XP_016869723.1:p.Arg122=
XM_017014235.1:c.1354A= XP_016869724.1:p.Arg452=
XR_001746171.1:n.2579A=
NM_139026.5:c.1261A= NP_620595.1:p.Arg421=
NM_139027.5:c.1354A= NP_620596.2:p.Arg452=
NM_139025.5:c.1354A= NP_620594.1:p.Arg452=
NM_139026.6:c.1261A= NP_620595.1:p.Arg421=
NM_139027.6:c.1354A= MANE Select NP_620596.2:p.Arg452=
NR_024514.3:n.995-2492A=