Canonical Allele Identifier: CA1882673597

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133437836G= , CM000671.2:g.133437836G=	GRCh38
NC_000009.10:g.135292777G=	NCBI36
NG_011934.2:g.28498G= , LRG_544:g.28498G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1523G= MANE Select	ENSP00000347927.2:p.Cys508=
ENST00000355699.6:c.1523G=	ENSP00000347927.2:p.Cys508=
ENST00000356589.6:c.1430G=	ENSP00000348997.2:p.Cys477=
ENST00000371916.5:c.779G=	ENSP00000360984.2:p.Cys260=
ENST00000371929.7:c.1523G=	ENSP00000360997.3:p.Cys508=
ENST00000474918.1:c.*327G=	ENSP00000435305.1:n.*327G=
ENST00000485925.5:n.974-1530G=
ENST00000495234.5:c.*807G=	ENSP00000435274.1:n.*807G=
NM_139025.4:c.1523G= , LRG_544t1:c.1523G=	NP_620594.1:p.Cys508=
NM_139026.4:c.1430G=	NP_620595.1:p.Cys477=
NM_139027.4:c.1523G=	NP_620596.2:p.Cys508=
NR_024514.2:n.993-1530G=
XM_011518174.1:c.1133G=	XP_011516476.1:p.Cys378=
XM_011518175.1:c.1523G=	XP_011516477.1:p.Cys508=
XM_011518176.1:c.539G=	XP_011516478.1:p.Cys180=
XM_011518177.1:c.533G=	XP_011516479.1:p.Cys178=
XM_011518178.1:c.188G=	XP_011516480.1:p.Cys63=
XM_011518179.1:c.309G=	XP_011516481.1:p.Val103=
XM_011518180.1:c.687-7027G=	XP_011516482.1:n.687-7027G=
XM_011518176.3:c.539G=	XP_011516478.1:p.Cys180=
XM_011518178.2:c.188G=	XP_011516480.1:p.Cys63=
XM_017014232.1:c.1511G=	XP_016869721.1:p.Cys504=
XM_017014233.1:c.1133G=	XP_016869722.1:p.Cys378=
XM_017014234.2:c.533G=	XP_016869723.1:p.Cys178=
XM_017014235.1:c.1523G=	XP_016869724.1:p.Cys508=
XR_001746171.1:n.2748G=
NM_139026.5:c.1430G=	NP_620595.1:p.Cys477=
NM_139027.5:c.1523G=	NP_620596.2:p.Cys508=
NM_139025.5:c.1523G=	NP_620594.1:p.Cys508=
NM_139026.6:c.1430G=	NP_620595.1:p.Cys477=
NM_139027.6:c.1523G= MANE Select	NP_620596.2:p.Cys508=
NR_024514.3:n.995-1530G=