Canonical Allele Identifier: CA1882681614

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454482G= , CM000671.2:g.133454482G=	GRCh38
NC_000009.10:g.135309425G=	NCBI36
NG_011934.2:g.45144G= , LRG_544:g.45144G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3112G= MANE Select	ENSP00000347927.2:p.Ala1038=
ENST00000355699.6:c.3112G=	ENSP00000347927.2:p.Ala1038=
ENST00000356589.6:c.3019G=	ENSP00000348997.2:p.Ala1007=
ENST00000371916.5:c.*581G=	ENSP00000360984.2:n.*581G=
ENST00000371929.7:c.3112G=	ENSP00000360997.3:p.Ala1038=
ENST00000485925.5:n.1928G=
NM_139025.4:c.3112G= , LRG_544t1:c.3112G=	NP_620594.1:p.Ala1038=
NM_139026.4:c.3019G=	NP_620595.1:p.Ala1007=
NM_139027.4:c.3112G=	NP_620596.2:p.Ala1038=
NR_024514.2:n.1947G=
XM_011518174.1:c.2722G=	XP_011516476.1:p.Ala908=
XM_011518175.1:c.3112G=	XP_011516477.1:p.Ala1038=
XM_011518176.1:c.2128G=	XP_011516478.1:p.Ala710=
XM_011518177.1:c.2122G=	XP_011516479.1:p.Ala708=
XM_011518178.1:c.1777G=	XP_011516480.1:p.Ala593=
XM_011518179.1:c.1777G=	XP_011516481.1:p.Ala593=
XM_011518180.1:c.1378G=	XP_011516482.1:p.Ala460=
XM_011518176.3:c.2128G=	XP_011516478.1:p.Ala710=
XM_011518178.2:c.1777G=	XP_011516480.1:p.Ala593=
XM_017014232.1:c.3100G=	XP_016869721.1:p.Ala1034=
XM_017014233.1:c.2722G=	XP_016869722.1:p.Ala908=
XM_017014234.2:c.2122G=	XP_016869723.1:p.Ala708=
NM_139026.5:c.3019G=	NP_620595.1:p.Ala1007=
NM_139027.5:c.3112G=	NP_620596.2:p.Ala1038=
NM_139025.5:c.3112G=	NP_620594.1:p.Ala1038=
NM_139026.6:c.3019G=	NP_620595.1:p.Ala1007=
NM_139027.6:c.3112G= MANE Select	NP_620596.2:p.Ala1038=
NR_024514.3:n.1949G=