Canonical Allele Identifier: CA1882673151

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436905C= , CM000671.2:g.133436905C=	GRCh38
NC_000009.10:g.135291846C=	NCBI36
NG_011934.2:g.27567C= , LRG_544:g.27567C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1385C= MANE Select	ENSP00000347927.2:p.Pro462=
ENST00000355699.6:c.1385C=	ENSP00000347927.2:p.Pro462=
ENST00000356589.6:c.1292C=	ENSP00000348997.2:p.Pro431=
ENST00000371916.5:c.641C=	ENSP00000360984.2:p.Pro214=
ENST00000371929.7:c.1385C=	ENSP00000360997.3:p.Pro462=
ENST00000474918.1:c.*189C=	ENSP00000435305.1:n.*189C=
ENST00000485925.5:n.974-2461C=
ENST00000495234.5:c.*669C=	ENSP00000435274.1:n.*669C=
NM_139025.4:c.1385C= , LRG_544t1:c.1385C=	NP_620594.1:p.Pro462=
NM_139026.4:c.1292C=	NP_620595.1:p.Pro431=
NM_139027.4:c.1385C=	NP_620596.2:p.Pro462=
NR_024514.2:n.993-2461C=
XM_011518174.1:c.995C=	XP_011516476.1:p.Pro332=
XM_011518175.1:c.1385C=	XP_011516477.1:p.Pro462=
XM_011518176.1:c.401C=	XP_011516478.1:p.Pro134=
XM_011518177.1:c.395C=	XP_011516479.1:p.Pro132=
XM_011518178.1:c.50C=	XP_011516480.1:p.Pro17=
XM_011518179.1:c.171C=	XP_011516481.1:p.Pro57=
XM_011518180.1:c.687-7958C=	XP_011516482.1:n.687-7958C=
XM_011518176.3:c.401C=	XP_011516478.1:p.Pro134=
XM_011518178.2:c.50C=	XP_011516480.1:p.Pro17=
XM_017014232.1:c.1373C=	XP_016869721.1:p.Pro458=
XM_017014233.1:c.995C=	XP_016869722.1:p.Pro332=
XM_017014234.2:c.395C=	XP_016869723.1:p.Pro132=
XM_017014235.1:c.1385C=	XP_016869724.1:p.Pro462=
XR_001746171.1:n.2610C=
NM_139026.5:c.1292C=	NP_620595.1:p.Pro431=
NM_139027.5:c.1385C=	NP_620596.2:p.Pro462=
NM_139025.5:c.1385C=	NP_620594.1:p.Pro462=
NM_139026.6:c.1292C=	NP_620595.1:p.Pro431=
NM_139027.6:c.1385C= MANE Select	NP_620596.2:p.Pro462=
NR_024514.3:n.995-2461C=