Canonical Allele Identifier: CA1882673130
Gene: ADAMTS13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436870C= , CM000671.2:g.133436870C= GRCh38
NC_000009.10:g.135291811C= NCBI36
NG_011934.2:g.27532C= , LRG_544:g.27532C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355699.7:c.1350C= MANE Select ENSP00000347927.2:p.Cys450=
ENST00000355699.6:c.1350C= ENSP00000347927.2:p.Cys450=
ENST00000356589.6:c.1257C= ENSP00000348997.2:p.Cys419=
ENST00000371916.5:c.606C= ENSP00000360984.2:p.Cys202=
ENST00000371929.7:c.1350C= ENSP00000360997.3:p.Cys450=
ENST00000474918.1:c.*154C= ENSP00000435305.1:n.*154C=
ENST00000485925.5:n.974-2496C=
ENST00000495234.5:c.*634C= ENSP00000435274.1:n.*634C=
NM_139025.4:c.1350C= , LRG_544t1:c.1350C= NP_620594.1:p.Cys450=
NM_139026.4:c.1257C= NP_620595.1:p.Cys419=
NM_139027.4:c.1350C= NP_620596.2:p.Cys450=
NR_024514.2:n.993-2496C=
XM_011518174.1:c.960C= XP_011516476.1:p.Cys320=
XM_011518175.1:c.1350C= XP_011516477.1:p.Cys450=
XM_011518176.1:c.366C= XP_011516478.1:p.Cys122=
XM_011518177.1:c.360C= XP_011516479.1:p.Cys120=
XM_011518178.1:c.15C= XP_011516480.1:p.Cys5=
XM_011518179.1:c.136C= XP_011516481.1:p.Arg46=
XM_011518180.1:c.687-7993C= XP_011516482.1:n.687-7993C=
XM_011518176.3:c.366C= XP_011516478.1:p.Cys122=
XM_011518178.2:c.15C= XP_011516480.1:p.Cys5=
XM_017014232.1:c.1338C= XP_016869721.1:p.Cys446=
XM_017014233.1:c.960C= XP_016869722.1:p.Cys320=
XM_017014234.2:c.360C= XP_016869723.1:p.Cys120=
XM_017014235.1:c.1350C= XP_016869724.1:p.Cys450=
XR_001746171.1:n.2575C=
NM_139026.5:c.1257C= NP_620595.1:p.Cys419=
NM_139027.5:c.1350C= NP_620596.2:p.Cys450=
NM_139025.5:c.1350C= NP_620594.1:p.Cys450=
NM_139026.6:c.1257C= NP_620595.1:p.Cys419=
NM_139027.6:c.1350C= MANE Select NP_620596.2:p.Cys450=
NR_024514.3:n.995-2496C=