Canonical Allele Identifier: CA1882673131
Gene: ADAMTS13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436871G= , CM000671.2:g.133436871G= GRCh38
NC_000009.10:g.135291812G= NCBI36
NG_011934.2:g.27533G= , LRG_544:g.27533G=

Transcript Alleles

HGVS Amino-acid change
ENST00000355699.7:c.1351G= MANE Select ENSP00000347927.2:p.Ala451=
ENST00000355699.6:c.1351G= ENSP00000347927.2:p.Ala451=
ENST00000356589.6:c.1258G= ENSP00000348997.2:p.Ala420=
ENST00000371916.5:c.607G= ENSP00000360984.2:p.Ala203=
ENST00000371929.7:c.1351G= ENSP00000360997.3:p.Ala451=
ENST00000474918.1:c.*155G= ENSP00000435305.1:n.*155G=
ENST00000485925.5:n.974-2495G=
ENST00000495234.5:c.*635G= ENSP00000435274.1:n.*635G=
NM_139025.4:c.1351G= , LRG_544t1:c.1351G= NP_620594.1:p.Ala451=
NM_139026.4:c.1258G= NP_620595.1:p.Ala420=
NM_139027.4:c.1351G= NP_620596.2:p.Ala451=
NR_024514.2:n.993-2495G=
XM_011518174.1:c.961G= XP_011516476.1:p.Ala321=
XM_011518175.1:c.1351G= XP_011516477.1:p.Ala451=
XM_011518176.1:c.367G= XP_011516478.1:p.Ala123=
XM_011518177.1:c.361G= XP_011516479.1:p.Ala121=
XM_011518178.1:c.16G= XP_011516480.1:p.Ala6=
XM_011518179.1:c.137G= XP_011516481.1:p.Arg46=
XM_011518180.1:c.687-7992G= XP_011516482.1:n.687-7992G=
XM_011518176.3:c.367G= XP_011516478.1:p.Ala123=
XM_011518178.2:c.16G= XP_011516480.1:p.Ala6=
XM_017014232.1:c.1339G= XP_016869721.1:p.Ala447=
XM_017014233.1:c.961G= XP_016869722.1:p.Ala321=
XM_017014234.2:c.361G= XP_016869723.1:p.Ala121=
XM_017014235.1:c.1351G= XP_016869724.1:p.Ala451=
XR_001746171.1:n.2576G=
NM_139026.5:c.1258G= NP_620595.1:p.Ala420=
NM_139027.5:c.1351G= NP_620596.2:p.Ala451=
NM_139025.5:c.1351G= NP_620594.1:p.Ala451=
NM_139026.6:c.1258G= NP_620595.1:p.Ala420=
NM_139027.6:c.1351G= MANE Select NP_620596.2:p.Ala451=
NR_024514.3:n.995-2495G=