Canonical Allele Identifier: CA1882673195

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436975G= , CM000671.2:g.133436975G=	GRCh38
NC_000009.10:g.135291916G=	NCBI36
NG_011934.2:g.27637G= , LRG_544:g.27637G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1435+20G= MANE Select	ENSP00000347927.2:n.1435+20G=
ENST00000355699.6:c.1435+20G=	ENSP00000347927.2:n.1435+20G=
ENST00000356589.6:c.1342+20G=	ENSP00000348997.2:n.1342+20G=
ENST00000371916.5:c.691+20G=	ENSP00000360984.2:n.691+20G=
ENST00000371929.7:c.1435+20G=	ENSP00000360997.3:n.1435+20G=
ENST00000474918.1:c.*239+20G=	ENSP00000435305.1:n.*239+20G=
ENST00000485925.5:n.974-2391G=
ENST00000495234.5:c.*719+20G=	ENSP00000435274.1:n.*719+20G=
NM_139025.4:c.1435+20G= , LRG_544t1:c.1435+20G=	NP_620594.1:n.1435+20G=
NM_139026.4:c.1342+20G=	NP_620595.1:n.1342+20G=
NM_139027.4:c.1435+20G=	NP_620596.2:n.1435+20G=
NR_024514.2:n.993-2391G=
XM_011518174.1:c.1045+20G=	XP_011516476.1:n.1045+20G=
XM_011518175.1:c.1435+20G=	XP_011516477.1:n.1435+20G=
XM_011518176.1:c.451+20G=	XP_011516478.1:n.451+20G=
XM_011518177.1:c.445+20G=	XP_011516479.1:n.445+20G=
XM_011518178.1:c.100+20G=	XP_011516480.1:n.100+20G=
XM_011518179.1:c.221+20G=	XP_011516481.1:n.221+20G=
XM_011518180.1:c.687-7888G=	XP_011516482.1:n.687-7888G=
XM_011518176.3:c.451+20G=	XP_011516478.1:n.451+20G=
XM_011518178.2:c.100+20G=	XP_011516480.1:n.100+20G=
XM_017014232.1:c.1423+20G=	XP_016869721.1:n.1423+20G=
XM_017014233.1:c.1045+20G=	XP_016869722.1:n.1045+20G=
XM_017014234.2:c.445+20G=	XP_016869723.1:n.445+20G=
XM_017014235.1:c.1435+20G=	XP_016869724.1:n.1435+20G=
XR_001746171.1:n.2660+20G=
NM_139026.5:c.1342+20G=	NP_620595.1:n.1342+20G=
NM_139027.5:c.1435+20G=	NP_620596.2:n.1435+20G=
NM_139025.5:c.1435+20G=	NP_620594.1:n.1435+20G=
NM_139026.6:c.1342+20G=	NP_620595.1:n.1342+20G=
NM_139027.6:c.1435+20G= MANE Select	NP_620596.2:n.1435+20G=
NR_024514.3:n.995-2391G=