Canonical Allele Identifier: CA1882681608

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454473C= , CM000671.2:g.133454473C=	GRCh38
NC_000009.10:g.135309416C=	NCBI36
NG_011934.2:g.45135C= , LRG_544:g.45135C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3103C= MANE Select	ENSP00000347927.2:p.Arg1035=
ENST00000355699.6:c.3103C=	ENSP00000347927.2:p.Arg1035=
ENST00000356589.6:c.3010C=	ENSP00000348997.2:p.Arg1004=
ENST00000371916.5:c.*572C=	ENSP00000360984.2:n.*572C=
ENST00000371929.7:c.3103C=	ENSP00000360997.3:p.Arg1035=
ENST00000485925.5:n.1919C=
NM_139025.4:c.3103C= , LRG_544t1:c.3103C=	NP_620594.1:p.Arg1035=
NM_139026.4:c.3010C=	NP_620595.1:p.Arg1004=
NM_139027.4:c.3103C=	NP_620596.2:p.Arg1035=
NR_024514.2:n.1938C=
XM_011518174.1:c.2713C=	XP_011516476.1:p.Arg905=
XM_011518175.1:c.3103C=	XP_011516477.1:p.Arg1035=
XM_011518176.1:c.2119C=	XP_011516478.1:p.Arg707=
XM_011518177.1:c.2113C=	XP_011516479.1:p.Arg705=
XM_011518178.1:c.1768C=	XP_011516480.1:p.Arg590=
XM_011518179.1:c.1768C=	XP_011516481.1:p.Arg590=
XM_011518180.1:c.1369C=	XP_011516482.1:p.Arg457=
XM_011518176.3:c.2119C=	XP_011516478.1:p.Arg707=
XM_011518178.2:c.1768C=	XP_011516480.1:p.Arg590=
XM_017014232.1:c.3091C=	XP_016869721.1:p.Arg1031=
XM_017014233.1:c.2713C=	XP_016869722.1:p.Arg905=
XM_017014234.2:c.2113C=	XP_016869723.1:p.Arg705=
NM_139026.5:c.3010C=	NP_620595.1:p.Arg1004=
NM_139027.5:c.3103C=	NP_620596.2:p.Arg1035=
NM_139025.5:c.3103C=	NP_620594.1:p.Arg1035=
NM_139026.6:c.3010C=	NP_620595.1:p.Arg1004=
NM_139027.6:c.3103C= MANE Select	NP_620596.2:p.Arg1035=
NR_024514.3:n.1940C=