Canonical Allele Identifier: CA1882677455

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133448724G= , CM000671.2:g.133448724G=	GRCh38
NC_000009.10:g.135303666G=	NCBI36
NG_011934.2:g.39386G= , LRG_544:g.39386G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.2857G= MANE Select	ENSP00000347927.2:p.Ala953=
ENST00000355699.6:c.2857G=	ENSP00000347927.2:p.Ala953=
ENST00000356589.6:c.2764G=	ENSP00000348997.2:p.Ala922=
ENST00000371916.5:c.*326G=	ENSP00000360984.2:n.*326G=
ENST00000371929.7:c.2857G=	ENSP00000360997.3:p.Ala953=
ENST00000485925.5:n.1673G=
ENST00000495234.5:c.*1689G=	ENSP00000435274.1:n.*1689G=
NM_139025.4:c.2857G= , LRG_544t1:c.2857G=	NP_620594.1:p.Ala953=
NM_139026.4:c.2764G=	NP_620595.1:p.Ala922=
NM_139027.4:c.2857G=	NP_620596.2:p.Ala953=
NR_024514.2:n.1692G=
XM_011518174.1:c.2467G=	XP_011516476.1:p.Ala823=
XM_011518175.1:c.2857G=	XP_011516477.1:p.Ala953=
XM_011518176.1:c.1873G=	XP_011516478.1:p.Ala625=
XM_011518177.1:c.1867G=	XP_011516479.1:p.Ala623=
XM_011518178.1:c.1522G=	XP_011516480.1:p.Ala508=
XM_011518179.1:c.1522G=	XP_011516481.1:p.Ala508=
XM_011518180.1:c.1123G=	XP_011516482.1:p.Ala375=
XM_011518176.3:c.1873G=	XP_011516478.1:p.Ala625=
XM_011518178.2:c.1522G=	XP_011516480.1:p.Ala508=
XM_017014232.1:c.2845G=	XP_016869721.1:p.Ala949=
XM_017014233.1:c.2467G=	XP_016869722.1:p.Ala823=
XM_017014234.2:c.1867G=	XP_016869723.1:p.Ala623=
XR_001746171.1:n.3630G=
NM_139026.5:c.2764G=	NP_620595.1:p.Ala922=
NM_139027.5:c.2857G=	NP_620596.2:p.Ala953=
NM_139025.5:c.2857G=	NP_620594.1:p.Ala953=
NM_139026.6:c.2764G=	NP_620595.1:p.Ala922=
NM_139027.6:c.2857G= MANE Select	NP_620596.2:p.Ala953=
NR_024514.3:n.1694G=