Canonical Allele Identifier: CA1882675980

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133440409C= , CM000671.2:g.133440409C=	GRCh38
NC_000009.10:g.135295351C=	NCBI36
NG_011934.2:g.31071C= , LRG_544:g.31071C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1852C= MANE Select	ENSP00000347927.2:p.Pro618=
ENST00000355699.6:c.1852C=	ENSP00000347927.2:p.Pro618=
ENST00000356589.6:c.1759C=	ENSP00000348997.2:p.Pro587=
ENST00000371916.5:c.1108C=	ENSP00000360984.2:p.Pro370=
ENST00000371929.7:c.1852C=	ENSP00000360997.3:p.Pro618=
ENST00000474918.1:c.*656C=	ENSP00000435305.1:n.*656C=
ENST00000485925.5:n.1120C=
ENST00000495234.5:c.*1136C=	ENSP00000435274.1:n.*1136C=
NM_139025.4:c.1852C= , LRG_544t1:c.1852C=	NP_620594.1:p.Pro618=
NM_139026.4:c.1759C=	NP_620595.1:p.Pro587=
NM_139027.4:c.1852C=	NP_620596.2:p.Pro618=
NR_024514.2:n.1139C=
XM_011518174.1:c.1462C=	XP_011516476.1:p.Pro488=
XM_011518175.1:c.1852C=	XP_011516477.1:p.Pro618=
XM_011518176.1:c.868C=	XP_011516478.1:p.Pro290=
XM_011518177.1:c.862C=	XP_011516479.1:p.Pro288=
XM_011518178.1:c.517C=	XP_011516480.1:p.Pro173=
XM_011518179.1:c.517C=	XP_011516481.1:p.Pro173=
XM_011518180.1:c.687-4454C=	XP_011516482.1:n.687-4454C=
XM_011518176.3:c.868C=	XP_011516478.1:p.Pro290=
XM_011518178.2:c.517C=	XP_011516480.1:p.Pro173=
XM_017014232.1:c.1840C=	XP_016869721.1:p.Pro614=
XM_017014233.1:c.1462C=	XP_016869722.1:p.Pro488=
XM_017014234.2:c.862C=	XP_016869723.1:p.Pro288=
XM_017014235.1:c.1852C=	XP_016869724.1:p.Pro618=
XR_001746171.1:n.3077C=
NM_139026.5:c.1759C=	NP_620595.1:p.Pro587=
NM_139027.5:c.1852C=	NP_620596.2:p.Pro618=
NM_139025.5:c.1852C=	NP_620594.1:p.Pro618=
NM_139026.6:c.1759C=	NP_620595.1:p.Pro587=
NM_139027.6:c.1852C= MANE Select	NP_620596.2:p.Pro618=
NR_024514.3:n.1141C=