Canonical Allele Identifier: CA1882682463

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133456160C= , CM000671.2:g.133456160C=	GRCh38
NC_000009.10:g.135311103C=	NCBI36
NG_011934.2:g.46822C= , LRG_544:g.46822C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3492C= MANE Select	ENSP00000347927.2:p.Pro1164=
ENST00000355699.6:c.3492C=	ENSP00000347927.2:p.Pro1164=
ENST00000356589.6:c.3399C=	ENSP00000348997.2:p.Pro1133=
ENST00000371910.1:c.48C=	ENSP00000360978.1:p.Pro16=
ENST00000371916.5:c.*961C=	ENSP00000360984.2:n.*961C=
ENST00000371929.7:c.3660C=	ENSP00000360997.3:p.Pro1220=
ENST00000485925.5:n.2308C=
NM_139025.4:c.3660C= , LRG_544t1:c.3660C=	NP_620594.1:p.Pro1220=
NM_139026.4:c.3399C=	NP_620595.1:p.Pro1133=
NM_139027.4:c.3492C=	NP_620596.2:p.Pro1164=
NR_024514.2:n.2327C=
XM_011518174.1:c.3270C=	XP_011516476.1:p.Pro1090=
XM_011518175.1:c.*67C=	XP_011516477.1:n.*67C=
XM_011518176.1:c.2676C=	XP_011516478.1:p.Pro892=
XM_011518177.1:c.2670C=	XP_011516479.1:p.Pro890=
XM_011518178.1:c.2325C=	XP_011516480.1:p.Pro775=
XM_011518179.1:c.2325C=	XP_011516481.1:p.Pro775=
XM_011518180.1:c.1926C=	XP_011516482.1:p.Pro642=
XM_011518176.3:c.2676C=	XP_011516478.1:p.Pro892=
XM_011518178.2:c.2325C=	XP_011516480.1:p.Pro775=
XM_017014232.1:c.3648C=	XP_016869721.1:p.Pro1216=
XM_017014233.1:c.3270C=	XP_016869722.1:p.Pro1090=
XM_017014234.2:c.2670C=	XP_016869723.1:p.Pro890=
NM_139026.5:c.3399C=	NP_620595.1:p.Pro1133=
NM_139027.5:c.3492C=	NP_620596.2:p.Pro1164=
NM_139025.5:c.3660C=	NP_620594.1:p.Pro1220=
NM_139026.6:c.3399C=	NP_620595.1:p.Pro1133=
NM_139027.6:c.3492C= MANE Select	NP_620596.2:p.Pro1164=
NR_024514.3:n.2329C=