Canonical Allele Identifier: CA1882671407

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133433478G= , CM000671.2:g.133433478G=	GRCh38
NC_000009.10:g.135288419G=	NCBI36
NG_011934.2:g.24140G= , LRG_544:g.24140G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1193G= MANE Select	ENSP00000347927.2:p.Arg398=
ENST00000355699.6:c.1193G=	ENSP00000347927.2:p.Arg398=
ENST00000356589.6:c.1100G=	ENSP00000348997.2:p.Arg367=
ENST00000371916.5:c.449G=	ENSP00000360984.2:p.Arg150=
ENST00000371929.7:c.1193G=	ENSP00000360997.3:p.Arg398=
ENST00000474918.1:c.*61G=	ENSP00000435305.1:n.*61G=
ENST00000485925.5:n.973+786G=
ENST00000495234.5:c.*477G=	ENSP00000435274.1:n.*477G=
NM_139025.4:c.1193G= , LRG_544t1:c.1193G=	NP_620594.1:p.Arg398=
NM_139026.4:c.1100G=	NP_620595.1:p.Arg367=
NM_139027.4:c.1193G=	NP_620596.2:p.Arg398=
NR_024514.2:n.992+786G=
XM_011518174.1:c.803G=	XP_011516476.1:p.Arg268=
XM_011518175.1:c.1193G=	XP_011516477.1:p.Arg398=
XM_011518176.1:c.209G=	XP_011516478.1:p.Arg70=
XM_011518177.1:c.203G=	XP_011516479.1:p.Arg68=
XM_011518178.1:c.-79G=	XP_011516480.1:n.-79G=
XM_011518179.1:c.43G=	XP_011516481.1:p.Ala15=
XM_011518180.1:c.686+7133G=	XP_011516482.1:n.686+7133G=
XM_011518176.3:c.209G=	XP_011516478.1:p.Arg70=
XM_011518178.2:c.-79G=	XP_011516480.1:n.-79G=
XM_017014232.1:c.1181G=	XP_016869721.1:p.Arg394=
XM_017014233.1:c.803G=	XP_016869722.1:p.Arg268=
XM_017014234.2:c.203G=	XP_016869723.1:p.Arg68=
XM_017014235.1:c.1193G=	XP_016869724.1:p.Arg398=
XR_001746171.1:n.2418G=
NM_139026.5:c.1100G=	NP_620595.1:p.Arg367=
NM_139027.5:c.1193G=	NP_620596.2:p.Arg398=
NM_139025.5:c.1193G=	NP_620594.1:p.Arg398=
NM_139026.6:c.1100G=	NP_620595.1:p.Arg367=
NM_139027.6:c.1193G= MANE Select	NP_620596.2:p.Arg398=
NR_024514.3:n.994+786G=