Canonical Allele Identifier: CA1882673180

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436952C= , CM000671.2:g.133436952C=	GRCh38
NC_000009.10:g.135291893C=	NCBI36
NG_011934.2:g.27614C= , LRG_544:g.27614C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1432C= MANE Select	ENSP00000347927.2:p.Gln478=
ENST00000355699.6:c.1432C=	ENSP00000347927.2:p.Gln478=
ENST00000356589.6:c.1339C=	ENSP00000348997.2:p.Gln447=
ENST00000371916.5:c.688C=	ENSP00000360984.2:p.Gln230=
ENST00000371929.7:c.1432C=	ENSP00000360997.3:p.Gln478=
ENST00000474918.1:c.*236C=	ENSP00000435305.1:n.*236C=
ENST00000485925.5:n.974-2414C=
ENST00000495234.5:c.*716C=	ENSP00000435274.1:n.*716C=
NM_139025.4:c.1432C= , LRG_544t1:c.1432C=	NP_620594.1:p.Gln478=
NM_139026.4:c.1339C=	NP_620595.1:p.Gln447=
NM_139027.4:c.1432C=	NP_620596.2:p.Gln478=
NR_024514.2:n.993-2414C=
XM_011518174.1:c.1042C=	XP_011516476.1:p.Gln348=
XM_011518175.1:c.1432C=	XP_011516477.1:p.Gln478=
XM_011518176.1:c.448C=	XP_011516478.1:p.Gln150=
XM_011518177.1:c.442C=	XP_011516479.1:p.Gln148=
XM_011518178.1:c.97C=	XP_011516480.1:p.Gln33=
XM_011518179.1:c.218C=	XP_011516481.1:p.Pro73=
XM_011518180.1:c.687-7911C=	XP_011516482.1:n.687-7911C=
XM_011518176.3:c.448C=	XP_011516478.1:p.Gln150=
XM_011518178.2:c.97C=	XP_011516480.1:p.Gln33=
XM_017014232.1:c.1420C=	XP_016869721.1:p.Gln474=
XM_017014233.1:c.1042C=	XP_016869722.1:p.Gln348=
XM_017014234.2:c.442C=	XP_016869723.1:p.Gln148=
XM_017014235.1:c.1432C=	XP_016869724.1:p.Gln478=
XR_001746171.1:n.2657C=
NM_139026.5:c.1339C=	NP_620595.1:p.Gln447=
NM_139027.5:c.1432C=	NP_620596.2:p.Gln478=
NM_139025.5:c.1432C=	NP_620594.1:p.Gln478=
NM_139026.6:c.1339C=	NP_620595.1:p.Gln447=
NM_139027.6:c.1432C= MANE Select	NP_620596.2:p.Gln478=
NR_024514.3:n.995-2414C=