Canonical Allele Identifier: CA1882678513

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133449794A= , CM000671.2:g.133449794A=	GRCh38
NC_000009.10:g.135304736A=	NCBI36
NG_011934.2:g.40456A= , LRG_544:g.40456A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2873A= MANE Select	ENSP00000347927.2:p.Lys958=
ENST00000355699.6:c.2873A=	ENSP00000347927.2:p.Lys958=
ENST00000356589.6:c.2780A=	ENSP00000348997.2:p.Lys927=
ENST00000371916.5:c.*342A=	ENSP00000360984.2:n.*342A=
ENST00000371929.7:c.2873A=	ENSP00000360997.3:p.Lys958=
ENST00000485925.5:n.1689A=
ENST00000495234.5:c.*1705A=	ENSP00000435274.1:n.*1705A=
NM_139025.4:c.2873A= , LRG_544t1:c.2873A=	NP_620594.1:p.Lys958=
NM_139026.4:c.2780A=	NP_620595.1:p.Lys927=
NM_139027.4:c.2873A=	NP_620596.2:p.Lys958=
NR_024514.2:n.1708A=
XM_011518174.1:c.2483A=	XP_011516476.1:p.Lys828=
XM_011518175.1:c.2873A=	XP_011516477.1:p.Lys958=
XM_011518176.1:c.1889A=	XP_011516478.1:p.Lys630=
XM_011518177.1:c.1883A=	XP_011516479.1:p.Lys628=
XM_011518178.1:c.1538A=	XP_011516480.1:p.Lys513=
XM_011518179.1:c.1538A=	XP_011516481.1:p.Lys513=
XM_011518180.1:c.1139A=	XP_011516482.1:p.Lys380=
XM_011518176.3:c.1889A=	XP_011516478.1:p.Lys630=
XM_011518178.2:c.1538A=	XP_011516480.1:p.Lys513=
XM_017014232.1:c.2861A=	XP_016869721.1:p.Lys954=
XM_017014233.1:c.2483A=	XP_016869722.1:p.Lys828=
XM_017014234.2:c.1883A=	XP_016869723.1:p.Lys628=
XR_001746171.1:n.3646A=
NM_139026.5:c.2780A=	NP_620595.1:p.Lys927=
NM_139027.5:c.2873A=	NP_620596.2:p.Lys958=
NM_139025.5:c.2873A=	NP_620594.1:p.Lys958=
NM_139026.6:c.2780A=	NP_620595.1:p.Lys927=
NM_139027.6:c.2873A= MANE Select	NP_620596.2:p.Lys958=
NR_024514.3:n.1710A=