Canonical Allele Identifier: CA1882681669

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454582A= , CM000671.2:g.133454582A=	GRCh38
NC_000009.10:g.135309525A=	NCBI36
NG_011934.2:g.45244A= , LRG_544:g.45244A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3212A= MANE Select	ENSP00000347927.2:p.Asp1071=
ENST00000355699.6:c.3212A=	ENSP00000347927.2:p.Asp1071=
ENST00000356589.6:c.3119A=	ENSP00000348997.2:p.Asp1040=
ENST00000371916.5:c.*681A=	ENSP00000360984.2:n.*681A=
ENST00000371929.7:c.3212A=	ENSP00000360997.3:p.Asp1071=
ENST00000485925.5:n.2028A=
NM_139025.4:c.3212A= , LRG_544t1:c.3212A=	NP_620594.1:p.Asp1071=
NM_139026.4:c.3119A=	NP_620595.1:p.Asp1040=
NM_139027.4:c.3212A=	NP_620596.2:p.Asp1071=
NR_024514.2:n.2047A=
XM_011518174.1:c.2822A=	XP_011516476.1:p.Asp941=
XM_011518175.1:c.3212A=	XP_011516477.1:p.Asp1071=
XM_011518176.1:c.2228A=	XP_011516478.1:p.Asp743=
XM_011518177.1:c.2222A=	XP_011516479.1:p.Asp741=
XM_011518178.1:c.1877A=	XP_011516480.1:p.Asp626=
XM_011518179.1:c.1877A=	XP_011516481.1:p.Asp626=
XM_011518180.1:c.1478A=	XP_011516482.1:p.Asp493=
XM_011518176.3:c.2228A=	XP_011516478.1:p.Asp743=
XM_011518178.2:c.1877A=	XP_011516480.1:p.Asp626=
XM_017014232.1:c.3200A=	XP_016869721.1:p.Asp1067=
XM_017014233.1:c.2822A=	XP_016869722.1:p.Asp941=
XM_017014234.2:c.2222A=	XP_016869723.1:p.Asp741=
NM_139026.5:c.3119A=	NP_620595.1:p.Asp1040=
NM_139027.5:c.3212A=	NP_620596.2:p.Asp1071=
NM_139025.5:c.3212A=	NP_620594.1:p.Asp1071=
NM_139026.6:c.3119A=	NP_620595.1:p.Asp1040=
NM_139027.6:c.3212A= MANE Select	NP_620596.2:p.Asp1071=
NR_024514.3:n.2049A=