Canonical Allele Identifier: CA1882673146
Gene: ADAMTS13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436897C= , CM000671.2:g.133436897C= GRCh38
NC_000009.10:g.135291838C= NCBI36
NG_011934.2:g.27559C= , LRG_544:g.27559C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355699.7:c.1377C= MANE Select ENSP00000347927.2:p.Arg459=
ENST00000355699.6:c.1377C= ENSP00000347927.2:p.Arg459=
ENST00000356589.6:c.1284C= ENSP00000348997.2:p.Arg428=
ENST00000371916.5:c.633C= ENSP00000360984.2:p.Arg211=
ENST00000371929.7:c.1377C= ENSP00000360997.3:p.Arg459=
ENST00000474918.1:c.*181C= ENSP00000435305.1:n.*181C=
ENST00000485925.5:n.974-2469C=
ENST00000495234.5:c.*661C= ENSP00000435274.1:n.*661C=
NM_139025.4:c.1377C= , LRG_544t1:c.1377C= NP_620594.1:p.Arg459=
NM_139026.4:c.1284C= NP_620595.1:p.Arg428=
NM_139027.4:c.1377C= NP_620596.2:p.Arg459=
NR_024514.2:n.993-2469C=
XM_011518174.1:c.987C= XP_011516476.1:p.Arg329=
XM_011518175.1:c.1377C= XP_011516477.1:p.Arg459=
XM_011518176.1:c.393C= XP_011516478.1:p.Arg131=
XM_011518177.1:c.387C= XP_011516479.1:p.Arg129=
XM_011518178.1:c.42C= XP_011516480.1:p.Arg14=
XM_011518179.1:c.163C= XP_011516481.1:p.Leu55=
XM_011518180.1:c.687-7966C= XP_011516482.1:n.687-7966C=
XM_011518176.3:c.393C= XP_011516478.1:p.Arg131=
XM_011518178.2:c.42C= XP_011516480.1:p.Arg14=
XM_017014232.1:c.1365C= XP_016869721.1:p.Arg455=
XM_017014233.1:c.987C= XP_016869722.1:p.Arg329=
XM_017014234.2:c.387C= XP_016869723.1:p.Arg129=
XM_017014235.1:c.1377C= XP_016869724.1:p.Arg459=
XR_001746171.1:n.2602C=
NM_139026.5:c.1284C= NP_620595.1:p.Arg428=
NM_139027.5:c.1377C= NP_620596.2:p.Arg459=
NM_139025.5:c.1377C= NP_620594.1:p.Arg459=
NM_139026.6:c.1284C= NP_620595.1:p.Arg428=
NM_139027.6:c.1377C= MANE Select NP_620596.2:p.Arg459=
NR_024514.3:n.995-2469C=