Canonical Allele Identifier: CA1882667598

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133426246C= , CM000671.2:g.133426246C=	GRCh38
NC_000009.10:g.135281187C=	NCBI36
NG_011934.2:g.16908C= , LRG_544:g.16908C=

Transcript Alleles

HGVS	Amino-acid Change
NM_139027.6:c.587C= MANE Select	NP_620596.2:p.Thr196=
ENST00000355699.7:c.587C= MANE Select	ENSP00000347927.2:p.Thr196=
NM_139025.4:c.587C= , LRG_544t1:c.587C=	NP_620594.1:p.Thr196=
NM_139025.5:c.587C=	NP_620594.1:p.Thr196=
NM_139026.4:c.587C=	NP_620595.1:p.Thr196=
NM_139026.5:c.587C=	NP_620595.1:p.Thr196=
NM_139026.6:c.587C=	NP_620595.1:p.Thr196=
NM_139027.4:c.587C=	NP_620596.2:p.Thr196=
NM_139027.5:c.587C=	NP_620596.2:p.Thr196=
NR_024514.2:n.788C=
NR_024514.3:n.790C=
ENST00000355699.6:c.587C=	ENSP00000347927.2:p.Thr196=
ENST00000356589.6:c.587C=	ENSP00000348997.2:p.Thr196=
ENST00000371911.7:c.587C=	ENSP00000360979.3:p.Thr196=
ENST00000371916.5:c.-158C=	ENSP00000360984.2:n.-158C=
ENST00000371929.7:c.587C=	ENSP00000360997.3:p.Thr196=
ENST00000474918.1:c.587C=	ENSP00000435305.1:p.Thr196=
ENST00000485925.5:n.769C=
ENST00000495234.5:c.587C=	ENSP00000435274.1:p.Thr196=
XM_011518174.1:c.197C=	XP_011516476.1:p.Thr66=
XM_011518175.1:c.587C=	XP_011516477.1:p.Thr196=
XM_011518180.1:c.587C=	XP_011516482.1:p.Thr196=
XM_017014232.1:c.575C=	XP_016869721.1:p.Thr192=
XM_017014233.1:c.197C=	XP_016869722.1:p.Thr66=
XM_017014234.2:c.-103C=	XP_016869723.1:n.-103C=
XM_017014235.1:c.587C=	XP_016869724.1:p.Thr196=
XR_001746171.1:n.1812C=