Canonical Allele Identifier: CA1882682427

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133456076T= , CM000671.2:g.133456076T=	GRCh38
NC_000009.10:g.135311019T=	NCBI36
NG_011934.2:g.46738T= , LRG_544:g.46738T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3408T= MANE Select	ENSP00000347927.2:p.Cys1136=
ENST00000355699.6:c.3408T=	ENSP00000347927.2:p.Cys1136=
ENST00000356589.6:c.3315T=	ENSP00000348997.2:p.Cys1105=
ENST00000371910.1:c.-37T=	ENSP00000360978.1:n.-37T=
ENST00000371916.5:c.*877T=	ENSP00000360984.2:n.*877T=
ENST00000371929.7:c.3576T=	ENSP00000360997.3:p.Cys1192=
ENST00000485925.5:n.2224T=
NM_139025.4:c.3576T= , LRG_544t1:c.3576T=	NP_620594.1:p.Cys1192=
NM_139026.4:c.3315T=	NP_620595.1:p.Cys1105=
NM_139027.4:c.3408T=	NP_620596.2:p.Cys1136=
NR_024514.2:n.2243T=
XM_011518174.1:c.3186T=	XP_011516476.1:p.Cys1062=
XM_011518175.1:c.3577T=	XP_011516477.1:p.Trp1193=
XM_011518176.1:c.2592T=	XP_011516478.1:p.Cys864=
XM_011518177.1:c.2586T=	XP_011516479.1:p.Cys862=
XM_011518178.1:c.2241T=	XP_011516480.1:p.Cys747=
XM_011518179.1:c.2241T=	XP_011516481.1:p.Cys747=
XM_011518180.1:c.1842T=	XP_011516482.1:p.Cys614=
XM_011518176.3:c.2592T=	XP_011516478.1:p.Cys864=
XM_011518178.2:c.2241T=	XP_011516480.1:p.Cys747=
XM_017014232.1:c.3564T=	XP_016869721.1:p.Cys1188=
XM_017014233.1:c.3186T=	XP_016869722.1:p.Cys1062=
XM_017014234.2:c.2586T=	XP_016869723.1:p.Cys862=
NM_139026.5:c.3315T=	NP_620595.1:p.Cys1105=
NM_139027.5:c.3408T=	NP_620596.2:p.Cys1136=
NM_139025.5:c.3576T=	NP_620594.1:p.Cys1192=
NM_139026.6:c.3315T=	NP_620595.1:p.Cys1105=
NM_139027.6:c.3408T= MANE Select	NP_620596.2:p.Cys1136=
NR_024514.3:n.2245T=