Canonical Allele Identifier: CA1882682438

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133456099C= , CM000671.2:g.133456099C=	GRCh38
NC_000009.10:g.135311042C=	NCBI36
NG_011934.2:g.46761C= , LRG_544:g.46761C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3431C= MANE Select	ENSP00000347927.2:p.Thr1144=
ENST00000355699.6:c.3431C=	ENSP00000347927.2:p.Thr1144=
ENST00000356589.6:c.3338C=	ENSP00000348997.2:p.Thr1113=
ENST00000371910.1:c.-14C=	ENSP00000360978.1:n.-14C=
ENST00000371916.5:c.*900C=	ENSP00000360984.2:n.*900C=
ENST00000371929.7:c.3599C=	ENSP00000360997.3:p.Thr1200=
ENST00000485925.5:n.2247C=
NM_139025.4:c.3599C= , LRG_544t1:c.3599C=	NP_620594.1:p.Thr1200=
NM_139026.4:c.3338C=	NP_620595.1:p.Thr1113=
NM_139027.4:c.3431C=	NP_620596.2:p.Thr1144=
NR_024514.2:n.2266C=
XM_011518174.1:c.3209C=	XP_011516476.1:p.Thr1070=
XM_011518175.1:c.*6C=	XP_011516477.1:n.*6C=
XM_011518176.1:c.2615C=	XP_011516478.1:p.Thr872=
XM_011518177.1:c.2609C=	XP_011516479.1:p.Thr870=
XM_011518178.1:c.2264C=	XP_011516480.1:p.Thr755=
XM_011518179.1:c.2264C=	XP_011516481.1:p.Thr755=
XM_011518180.1:c.1865C=	XP_011516482.1:p.Thr622=
XM_011518176.3:c.2615C=	XP_011516478.1:p.Thr872=
XM_011518178.2:c.2264C=	XP_011516480.1:p.Thr755=
XM_017014232.1:c.3587C=	XP_016869721.1:p.Thr1196=
XM_017014233.1:c.3209C=	XP_016869722.1:p.Thr1070=
XM_017014234.2:c.2609C=	XP_016869723.1:p.Thr870=
NM_139026.5:c.3338C=	NP_620595.1:p.Thr1113=
NM_139027.5:c.3431C=	NP_620596.2:p.Thr1144=
NM_139025.5:c.3599C=	NP_620594.1:p.Thr1200=
NM_139026.6:c.3338C=	NP_620595.1:p.Thr1113=
NM_139027.6:c.3431C= MANE Select	NP_620596.2:p.Thr1144=
NR_024514.3:n.2268C=