Canonical Allele Identifier: CA1882673264

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133437116C= , CM000671.2:g.133437116C=	GRCh38
NC_000009.10:g.135292057C=	NCBI36
NG_011934.2:g.27778C= , LRG_544:g.27778C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1435+161C= MANE Select	ENSP00000347927.2:n.1435+161C=
ENST00000355699.6:c.1435+161C=	ENSP00000347927.2:n.1435+161C=
ENST00000356589.6:c.1342+161C=	ENSP00000348997.2:n.1342+161C=
ENST00000371916.5:c.691+161C=	ENSP00000360984.2:n.691+161C=
ENST00000371929.7:c.1435+161C=	ENSP00000360997.3:n.1435+161C=
ENST00000474918.1:c.*239+161C=	ENSP00000435305.1:n.*239+161C=
ENST00000485925.5:n.974-2250C=
ENST00000495234.5:c.*719+161C=	ENSP00000435274.1:n.*719+161C=
NM_139025.4:c.1435+161C= , LRG_544t1:c.1435+161C=	NP_620594.1:n.1435+161C=
NM_139026.4:c.1342+161C=	NP_620595.1:n.1342+161C=
NM_139027.4:c.1435+161C=	NP_620596.2:n.1435+161C=
NR_024514.2:n.993-2250C=
XM_011518174.1:c.1045+161C=	XP_011516476.1:n.1045+161C=
XM_011518175.1:c.1435+161C=	XP_011516477.1:n.1435+161C=
XM_011518176.1:c.451+161C=	XP_011516478.1:n.451+161C=
XM_011518177.1:c.445+161C=	XP_011516479.1:n.445+161C=
XM_011518178.1:c.100+161C=	XP_011516480.1:n.100+161C=
XM_011518179.1:c.221+161C=	XP_011516481.1:n.221+161C=
XM_011518180.1:c.687-7747C=	XP_011516482.1:n.687-7747C=
XM_011518176.3:c.451+161C=	XP_011516478.1:n.451+161C=
XM_011518178.2:c.100+161C=	XP_011516480.1:n.100+161C=
XM_017014232.1:c.1423+161C=	XP_016869721.1:n.1423+161C=
XM_017014233.1:c.1045+161C=	XP_016869722.1:n.1045+161C=
XM_017014234.2:c.445+161C=	XP_016869723.1:n.445+161C=
XM_017014235.1:c.1435+161C=	XP_016869724.1:n.1435+161C=
XR_001746171.1:n.2660+161C=
NM_139026.5:c.1342+161C=	NP_620595.1:n.1342+161C=
NM_139027.5:c.1435+161C=	NP_620596.2:n.1435+161C=
NM_139025.5:c.1435+161C=	NP_620594.1:n.1435+161C=
NM_139026.6:c.1342+161C=	NP_620595.1:n.1342+161C=
NM_139027.6:c.1435+161C= MANE Select	NP_620596.2:n.1435+161C=
NR_024514.3:n.995-2250C=