Canonical Allele Identifier: CA1882678558

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133449813G= , CM000671.2:g.133449813G=	GRCh38
NC_000009.10:g.135304755G=	NCBI36
NG_011934.2:g.40475G= , LRG_544:g.40475G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2892G= MANE Select	ENSP00000347927.2:p.Val964=
ENST00000355699.6:c.2892G=	ENSP00000347927.2:p.Val964=
ENST00000356589.6:c.2799G=	ENSP00000348997.2:p.Val933=
ENST00000371916.5:c.*361G=	ENSP00000360984.2:n.*361G=
ENST00000371929.7:c.2892G=	ENSP00000360997.3:p.Val964=
ENST00000485925.5:n.1708G=
ENST00000495234.5:c.*1724G=	ENSP00000435274.1:n.*1724G=
NM_139025.4:c.2892G= , LRG_544t1:c.2892G=	NP_620594.1:p.Val964=
NM_139026.4:c.2799G=	NP_620595.1:p.Val933=
NM_139027.4:c.2892G=	NP_620596.2:p.Val964=
NR_024514.2:n.1727G=
XM_011518174.1:c.2502G=	XP_011516476.1:p.Val834=
XM_011518175.1:c.2892G=	XP_011516477.1:p.Val964=
XM_011518176.1:c.1908G=	XP_011516478.1:p.Val636=
XM_011518177.1:c.1902G=	XP_011516479.1:p.Val634=
XM_011518178.1:c.1557G=	XP_011516480.1:p.Val519=
XM_011518179.1:c.1557G=	XP_011516481.1:p.Val519=
XM_011518180.1:c.1158G=	XP_011516482.1:p.Val386=
XM_011518176.3:c.1908G=	XP_011516478.1:p.Val636=
XM_011518178.2:c.1557G=	XP_011516480.1:p.Val519=
XM_017014232.1:c.2880G=	XP_016869721.1:p.Val960=
XM_017014233.1:c.2502G=	XP_016869722.1:p.Val834=
XM_017014234.2:c.1902G=	XP_016869723.1:p.Val634=
XR_001746171.1:n.3665G=
NM_139026.5:c.2799G=	NP_620595.1:p.Val933=
NM_139027.5:c.2892G=	NP_620596.2:p.Val964=
NM_139025.5:c.2892G=	NP_620594.1:p.Val964=
NM_139026.6:c.2799G=	NP_620595.1:p.Val933=
NM_139027.6:c.2892G= MANE Select	NP_620596.2:p.Val964=
NR_024514.3:n.1729G=