Canonical Allele Identifier: CA1882673140
Gene: ADAMTS13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133436888G= , CM000671.2:g.133436888G= GRCh38
NC_000009.10:g.135291829G= NCBI36
NG_011934.2:g.27550G= , LRG_544:g.27550G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355699.7:c.1368G= MANE Select ENSP00000347927.2:p.Gln456=
ENST00000355699.6:c.1368G= ENSP00000347927.2:p.Gln456=
ENST00000356589.6:c.1275G= ENSP00000348997.2:p.Gln425=
ENST00000371916.5:c.624G= ENSP00000360984.2:p.Gln208=
ENST00000371929.7:c.1368G= ENSP00000360997.3:p.Gln456=
ENST00000474918.1:c.*172G= ENSP00000435305.1:n.*172G=
ENST00000485925.5:n.974-2478G=
ENST00000495234.5:c.*652G= ENSP00000435274.1:n.*652G=
NM_139025.4:c.1368G= , LRG_544t1:c.1368G= NP_620594.1:p.Gln456=
NM_139026.4:c.1275G= NP_620595.1:p.Gln425=
NM_139027.4:c.1368G= NP_620596.2:p.Gln456=
NR_024514.2:n.993-2478G=
XM_011518174.1:c.978G= XP_011516476.1:p.Gln326=
XM_011518175.1:c.1368G= XP_011516477.1:p.Gln456=
XM_011518176.1:c.384G= XP_011516478.1:p.Gln128=
XM_011518177.1:c.378G= XP_011516479.1:p.Gln126=
XM_011518178.1:c.33G= XP_011516480.1:p.Gln11=
XM_011518179.1:c.154G= XP_011516481.1:p.Ala52=
XM_011518180.1:c.687-7975G= XP_011516482.1:n.687-7975G=
XM_011518176.3:c.384G= XP_011516478.1:p.Gln128=
XM_011518178.2:c.33G= XP_011516480.1:p.Gln11=
XM_017014232.1:c.1356G= XP_016869721.1:p.Gln452=
XM_017014233.1:c.978G= XP_016869722.1:p.Gln326=
XM_017014234.2:c.378G= XP_016869723.1:p.Gln126=
XM_017014235.1:c.1368G= XP_016869724.1:p.Gln456=
XR_001746171.1:n.2593G=
NM_139026.5:c.1275G= NP_620595.1:p.Gln425=
NM_139027.5:c.1368G= NP_620596.2:p.Gln456=
NM_139025.5:c.1368G= NP_620594.1:p.Gln456=
NM_139026.6:c.1275G= NP_620595.1:p.Gln425=
NM_139027.6:c.1368G= MANE Select NP_620596.2:p.Gln456=
NR_024514.3:n.995-2478G=