Canonical Allele Identifier: CA1882681605

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454465C= , CM000671.2:g.133454465C=	GRCh38
NC_000009.10:g.135309408C=	NCBI36
NG_011934.2:g.45127C= , LRG_544:g.45127C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.3095C= MANE Select	ENSP00000347927.2:p.Thr1032=
ENST00000355699.6:c.3095C=	ENSP00000347927.2:p.Thr1032=
ENST00000356589.6:c.3002C=	ENSP00000348997.2:p.Thr1001=
ENST00000371916.5:c.*564C=	ENSP00000360984.2:n.*564C=
ENST00000371929.7:c.3095C=	ENSP00000360997.3:p.Thr1032=
ENST00000485925.5:n.1911C=
NM_139025.4:c.3095C= , LRG_544t1:c.3095C=	NP_620594.1:p.Thr1032=
NM_139026.4:c.3002C=	NP_620595.1:p.Thr1001=
NM_139027.4:c.3095C=	NP_620596.2:p.Thr1032=
NR_024514.2:n.1930C=
XM_011518174.1:c.2705C=	XP_011516476.1:p.Thr902=
XM_011518175.1:c.3095C=	XP_011516477.1:p.Thr1032=
XM_011518176.1:c.2111C=	XP_011516478.1:p.Thr704=
XM_011518177.1:c.2105C=	XP_011516479.1:p.Thr702=
XM_011518178.1:c.1760C=	XP_011516480.1:p.Thr587=
XM_011518179.1:c.1760C=	XP_011516481.1:p.Thr587=
XM_011518180.1:c.1361C=	XP_011516482.1:p.Thr454=
XM_011518176.3:c.2111C=	XP_011516478.1:p.Thr704=
XM_011518178.2:c.1760C=	XP_011516480.1:p.Thr587=
XM_017014232.1:c.3083C=	XP_016869721.1:p.Thr1028=
XM_017014233.1:c.2705C=	XP_016869722.1:p.Thr902=
XM_017014234.2:c.2105C=	XP_016869723.1:p.Thr702=
XR_001746171.1:n.3868C=
NM_139026.5:c.3002C=	NP_620595.1:p.Thr1001=
NM_139027.5:c.3095C=	NP_620596.2:p.Thr1032=
NM_139025.5:c.3095C=	NP_620594.1:p.Thr1032=
NM_139026.6:c.3002C=	NP_620595.1:p.Thr1001=
NM_139027.6:c.3095C= MANE Select	NP_620596.2:p.Thr1032=
NR_024514.3:n.1932C=