Canonical Allele Identifier: CA1882673179

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436949A= , CM000671.2:g.133436949A=	GRCh38
NC_000009.10:g.135291890A=	NCBI36
NG_011934.2:g.27611A= , LRG_544:g.27611A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1429A= MANE Select	ENSP00000347927.2:p.Ser477=
ENST00000355699.6:c.1429A=	ENSP00000347927.2:p.Ser477=
ENST00000356589.6:c.1336A=	ENSP00000348997.2:p.Ser446=
ENST00000371916.5:c.685A=	ENSP00000360984.2:p.Ser229=
ENST00000371929.7:c.1429A=	ENSP00000360997.3:p.Ser477=
ENST00000474918.1:c.*233A=	ENSP00000435305.1:n.*233A=
ENST00000485925.5:n.974-2417A=
ENST00000495234.5:c.*713A=	ENSP00000435274.1:n.*713A=
NM_139025.4:c.1429A= , LRG_544t1:c.1429A=	NP_620594.1:p.Ser477=
NM_139026.4:c.1336A=	NP_620595.1:p.Ser446=
NM_139027.4:c.1429A=	NP_620596.2:p.Ser477=
NR_024514.2:n.993-2417A=
XM_011518174.1:c.1039A=	XP_011516476.1:p.Ser347=
XM_011518175.1:c.1429A=	XP_011516477.1:p.Ser477=
XM_011518176.1:c.445A=	XP_011516478.1:p.Ser149=
XM_011518177.1:c.439A=	XP_011516479.1:p.Ser147=
XM_011518178.1:c.94A=	XP_011516480.1:p.Ser32=
XM_011518179.1:c.215A=	XP_011516481.1:p.Gln72=
XM_011518180.1:c.687-7914A=	XP_011516482.1:n.687-7914A=
XM_011518176.3:c.445A=	XP_011516478.1:p.Ser149=
XM_011518178.2:c.94A=	XP_011516480.1:p.Ser32=
XM_017014232.1:c.1417A=	XP_016869721.1:p.Ser473=
XM_017014233.1:c.1039A=	XP_016869722.1:p.Ser347=
XM_017014234.2:c.439A=	XP_016869723.1:p.Ser147=
XM_017014235.1:c.1429A=	XP_016869724.1:p.Ser477=
XR_001746171.1:n.2654A=
NM_139026.5:c.1336A=	NP_620595.1:p.Ser446=
NM_139027.5:c.1429A=	NP_620596.2:p.Ser477=
NM_139025.5:c.1429A=	NP_620594.1:p.Ser477=
NM_139026.6:c.1336A=	NP_620595.1:p.Ser446=
NM_139027.6:c.1429A= MANE Select	NP_620596.2:p.Ser477=
NR_024514.3:n.995-2417A=