Canonical Allele Identifier: CA1882673176

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436946C= , CM000671.2:g.133436946C=	GRCh38
NC_000009.10:g.135291887C=	NCBI36
NG_011934.2:g.27608C= , LRG_544:g.27608C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1426C= MANE Select	ENSP00000347927.2:p.His476=
ENST00000355699.6:c.1426C=	ENSP00000347927.2:p.His476=
ENST00000356589.6:c.1333C=	ENSP00000348997.2:p.His445=
ENST00000371916.5:c.682C=	ENSP00000360984.2:p.His228=
ENST00000371929.7:c.1426C=	ENSP00000360997.3:p.His476=
ENST00000474918.1:c.*230C=	ENSP00000435305.1:n.*230C=
ENST00000485925.5:n.974-2420C=
ENST00000495234.5:c.*710C=	ENSP00000435274.1:n.*710C=
NM_139025.4:c.1426C= , LRG_544t1:c.1426C=	NP_620594.1:p.His476=
NM_139026.4:c.1333C=	NP_620595.1:p.His445=
NM_139027.4:c.1426C=	NP_620596.2:p.His476=
NR_024514.2:n.993-2420C=
XM_011518174.1:c.1036C=	XP_011516476.1:p.His346=
XM_011518175.1:c.1426C=	XP_011516477.1:p.His476=
XM_011518176.1:c.442C=	XP_011516478.1:p.His148=
XM_011518177.1:c.436C=	XP_011516479.1:p.His146=
XM_011518178.1:c.91C=	XP_011516480.1:p.His31=
XM_011518179.1:c.212C=	XP_011516481.1:p.Thr71=
XM_011518180.1:c.687-7917C=	XP_011516482.1:n.687-7917C=
XM_011518176.3:c.442C=	XP_011516478.1:p.His148=
XM_011518178.2:c.91C=	XP_011516480.1:p.His31=
XM_017014232.1:c.1414C=	XP_016869721.1:p.His472=
XM_017014233.1:c.1036C=	XP_016869722.1:p.His346=
XM_017014234.2:c.436C=	XP_016869723.1:p.His146=
XM_017014235.1:c.1426C=	XP_016869724.1:p.His476=
XR_001746171.1:n.2651C=
NM_139026.5:c.1333C=	NP_620595.1:p.His445=
NM_139027.5:c.1426C=	NP_620596.2:p.His476=
NM_139025.5:c.1426C=	NP_620594.1:p.His476=
NM_139026.6:c.1333C=	NP_620595.1:p.His445=
NM_139027.6:c.1426C= MANE Select	NP_620596.2:p.His476=
NR_024514.3:n.995-2420C=