Canonical Allele Identifier: CA1882677447

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133448721C= , CM000671.2:g.133448721C=	GRCh38
NC_000009.10:g.135303663C=	NCBI36
NG_011934.2:g.39383C= , LRG_544:g.39383C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.2854C= MANE Select	ENSP00000347927.2:p.Pro952=
ENST00000355699.6:c.2854C=	ENSP00000347927.2:p.Pro952=
ENST00000356589.6:c.2761C=	ENSP00000348997.2:p.Pro921=
ENST00000371916.5:c.*323C=	ENSP00000360984.2:n.*323C=
ENST00000371929.7:c.2854C=	ENSP00000360997.3:p.Pro952=
ENST00000485925.5:n.1670C=
ENST00000495234.5:c.*1686C=	ENSP00000435274.1:n.*1686C=
NM_139025.4:c.2854C= , LRG_544t1:c.2854C=	NP_620594.1:p.Pro952=
NM_139026.4:c.2761C=	NP_620595.1:p.Pro921=
NM_139027.4:c.2854C=	NP_620596.2:p.Pro952=
NR_024514.2:n.1689C=
XM_011518174.1:c.2464C=	XP_011516476.1:p.Pro822=
XM_011518175.1:c.2854C=	XP_011516477.1:p.Pro952=
XM_011518176.1:c.1870C=	XP_011516478.1:p.Pro624=
XM_011518177.1:c.1864C=	XP_011516479.1:p.Pro622=
XM_011518178.1:c.1519C=	XP_011516480.1:p.Pro507=
XM_011518179.1:c.1519C=	XP_011516481.1:p.Pro507=
XM_011518180.1:c.1120C=	XP_011516482.1:p.Pro374=
XM_011518176.3:c.1870C=	XP_011516478.1:p.Pro624=
XM_011518178.2:c.1519C=	XP_011516480.1:p.Pro507=
XM_017014232.1:c.2842C=	XP_016869721.1:p.Pro948=
XM_017014233.1:c.2464C=	XP_016869722.1:p.Pro822=
XM_017014234.2:c.1864C=	XP_016869723.1:p.Pro622=
XR_001746171.1:n.3627C=
NM_139026.5:c.2761C=	NP_620595.1:p.Pro921=
NM_139027.5:c.2854C=	NP_620596.2:p.Pro952=
NM_139025.5:c.2854C=	NP_620594.1:p.Pro952=
NM_139026.6:c.2761C=	NP_620595.1:p.Pro921=
NM_139027.6:c.2854C= MANE Select	NP_620596.2:p.Pro952=
NR_024514.3:n.1691C=