Canonical Allele Identifier: CA1882681643

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454535T= , CM000671.2:g.133454535T=	GRCh38
NC_000009.10:g.135309478T=	NCBI36
NG_011934.2:g.45197T= , LRG_544:g.45197T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3165T= MANE Select	ENSP00000347927.2:p.Cys1055=
ENST00000355699.6:c.3165T=	ENSP00000347927.2:p.Cys1055=
ENST00000356589.6:c.3072T=	ENSP00000348997.2:p.Cys1024=
ENST00000371916.5:c.*634T=	ENSP00000360984.2:n.*634T=
ENST00000371929.7:c.3165T=	ENSP00000360997.3:p.Cys1055=
ENST00000485925.5:n.1981T=
NM_139025.4:c.3165T= , LRG_544t1:c.3165T=	NP_620594.1:p.Cys1055=
NM_139026.4:c.3072T=	NP_620595.1:p.Cys1024=
NM_139027.4:c.3165T=	NP_620596.2:p.Cys1055=
NR_024514.2:n.2000T=
XM_011518174.1:c.2775T=	XP_011516476.1:p.Cys925=
XM_011518175.1:c.3165T=	XP_011516477.1:p.Cys1055=
XM_011518176.1:c.2181T=	XP_011516478.1:p.Cys727=
XM_011518177.1:c.2175T=	XP_011516479.1:p.Cys725=
XM_011518178.1:c.1830T=	XP_011516480.1:p.Cys610=
XM_011518179.1:c.1830T=	XP_011516481.1:p.Cys610=
XM_011518180.1:c.1431T=	XP_011516482.1:p.Cys477=
XM_011518176.3:c.2181T=	XP_011516478.1:p.Cys727=
XM_011518178.2:c.1830T=	XP_011516480.1:p.Cys610=
XM_017014232.1:c.3153T=	XP_016869721.1:p.Cys1051=
XM_017014233.1:c.2775T=	XP_016869722.1:p.Cys925=
XM_017014234.2:c.2175T=	XP_016869723.1:p.Cys725=
NM_139026.5:c.3072T=	NP_620595.1:p.Cys1024=
NM_139027.5:c.3165T=	NP_620596.2:p.Cys1055=
NM_139025.5:c.3165T=	NP_620594.1:p.Cys1055=
NM_139026.6:c.3072T=	NP_620595.1:p.Cys1024=
NM_139027.6:c.3165T= MANE Select	NP_620596.2:p.Cys1055=
NR_024514.3:n.2002T=