Canonical Allele Identifier: CA1882666689

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133424452C= , CM000671.2:g.133424452C=	GRCh38
NC_000009.10:g.135279393C=	NCBI36
NG_011934.2:g.15114C= , LRG_544:g.15114C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.304C= MANE Select	ENSP00000347927.2:p.Arg102=
ENST00000355699.6:c.304C=	ENSP00000347927.2:p.Arg102=
ENST00000356589.6:c.304C=	ENSP00000348997.2:p.Arg102=
ENST00000371911.7:c.304C=	ENSP00000360979.3:p.Arg102=
ENST00000371916.5:c.-441C=	ENSP00000360984.2:n.-441C=
ENST00000371929.7:c.304C=	ENSP00000360997.3:p.Arg102=
ENST00000474918.1:c.304C=	ENSP00000435305.1:p.Arg102=
ENST00000485925.5:n.486C=
ENST00000495234.5:c.304C=	ENSP00000435274.1:p.Arg102=
NM_139025.4:c.304C= , LRG_544t1:c.304C=	NP_620594.1:p.Arg102=
NM_139026.4:c.304C=	NP_620595.1:p.Arg102=
NM_139027.4:c.304C=	NP_620596.2:p.Arg102=
NR_024514.2:n.505C=
XM_011518174.1:c.-87C=	XP_011516476.1:n.-87C=
XM_011518175.1:c.304C=	XP_011516477.1:p.Arg102=
XM_011518180.1:c.304C=	XP_011516482.1:p.Arg102=
XM_017014232.1:c.292C=	XP_016869721.1:p.Arg98=
XM_017014233.1:c.-87C=	XP_016869722.1:n.-87C=
XM_017014235.1:c.304C=	XP_016869724.1:p.Arg102=
XR_001746171.1:n.1529C=
NM_139026.5:c.304C=	NP_620595.1:p.Arg102=
NM_139027.5:c.304C=	NP_620596.2:p.Arg102=
NM_139025.5:c.304C=	NP_620594.1:p.Arg102=
NM_139026.6:c.304C=	NP_620595.1:p.Arg102=
NM_139027.6:c.304C= MANE Select	NP_620596.2:p.Arg102=
NR_024514.3:n.507C=