Canonical Allele Identifier: CA1882681587

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454424C= , CM000671.2:g.133454424C=	GRCh38
NC_000009.10:g.135309367C=	NCBI36
NG_011934.2:g.45086C= , LRG_544:g.45086C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3054C= MANE Select	ENSP00000347927.2:p.Val1018=
ENST00000355699.6:c.3054C=	ENSP00000347927.2:p.Val1018=
ENST00000356589.6:c.2961C=	ENSP00000348997.2:p.Val987=
ENST00000371916.5:c.*523C=	ENSP00000360984.2:n.*523C=
ENST00000371929.7:c.3054C=	ENSP00000360997.3:p.Val1018=
ENST00000485925.5:n.1870C=
NM_139025.4:c.3054C= , LRG_544t1:c.3054C=	NP_620594.1:p.Val1018=
NM_139026.4:c.2961C=	NP_620595.1:p.Val987=
NM_139027.4:c.3054C=	NP_620596.2:p.Val1018=
NR_024514.2:n.1889C=
XM_011518174.1:c.2664C=	XP_011516476.1:p.Val888=
XM_011518175.1:c.3054C=	XP_011516477.1:p.Val1018=
XM_011518176.1:c.2070C=	XP_011516478.1:p.Val690=
XM_011518177.1:c.2064C=	XP_011516479.1:p.Val688=
XM_011518178.1:c.1719C=	XP_011516480.1:p.Val573=
XM_011518179.1:c.1719C=	XP_011516481.1:p.Val573=
XM_011518180.1:c.1320C=	XP_011516482.1:p.Val440=
XM_011518176.3:c.2070C=	XP_011516478.1:p.Val690=
XM_011518178.2:c.1719C=	XP_011516480.1:p.Val573=
XM_017014232.1:c.3042C=	XP_016869721.1:p.Val1014=
XM_017014233.1:c.2664C=	XP_016869722.1:p.Val888=
XM_017014234.2:c.2064C=	XP_016869723.1:p.Val688=
XR_001746171.1:n.3827C=
NM_139026.5:c.2961C=	NP_620595.1:p.Val987=
NM_139027.5:c.3054C=	NP_620596.2:p.Val1018=
NM_139025.5:c.3054C=	NP_620594.1:p.Val1018=
NM_139026.6:c.2961C=	NP_620595.1:p.Val987=
NM_139027.6:c.3054C= MANE Select	NP_620596.2:p.Val1018=
NR_024514.3:n.1891C=