Canonical Allele Identifier: CA2692373010

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133448727-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133448727C>A , CM000671.2:g.133448727C>A	GRCh38
NC_000009.10:g.135303669C>A	NCBI36
NG_011934.2:g.39389C>A , LRG_544:g.39389C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.2860C>A MANE Select	ENSP00000347927.2:p.Arg954=
ENST00000355699.6:c.2860C>A	ENSP00000347927.2:p.Arg954=
ENST00000356589.6:c.2767C>A	ENSP00000348997.2:p.Arg923=
ENST00000371916.5:c.*329C>A	ENSP00000360984.2:n.*329C>A
ENST00000371929.7:c.2860C>A	ENSP00000360997.3:p.Arg954=
ENST00000485925.5:n.1676C>A
ENST00000495234.5:c.*1692C>A	ENSP00000435274.1:n.*1692C>A
NM_139025.4:c.2860C>A , LRG_544t1:c.2860C>A	NP_620594.1:p.Arg954=
NM_139026.4:c.2767C>A	NP_620595.1:p.Arg923=
NM_139027.4:c.2860C>A	NP_620596.2:p.Arg954=
NR_024514.2:n.1695C>A
XM_011518174.1:c.2470C>A	XP_011516476.1:p.Arg824=
XM_011518175.1:c.2860C>A	XP_011516477.1:p.Arg954=
XM_011518176.1:c.1876C>A	XP_011516478.1:p.Arg626=
XM_011518177.1:c.1870C>A	XP_011516479.1:p.Arg624=
XM_011518178.1:c.1525C>A	XP_011516480.1:p.Arg509=
XM_011518179.1:c.1525C>A	XP_011516481.1:p.Arg509=
XM_011518180.1:c.1126C>A	XP_011516482.1:p.Arg376=
XM_011518176.3:c.1876C>A	XP_011516478.1:p.Arg626=
XM_011518178.2:c.1525C>A	XP_011516480.1:p.Arg509=
XM_017014232.1:c.2848C>A	XP_016869721.1:p.Arg950=
XM_017014233.1:c.2470C>A	XP_016869722.1:p.Arg824=
XM_017014234.2:c.1870C>A	XP_016869723.1:p.Arg624=
XR_001746171.1:n.3633C>A
NM_139026.5:c.2767C>A	NP_620595.1:p.Arg923=
NM_139027.5:c.2860C>A	NP_620596.2:p.Arg954=
NM_139025.5:c.2860C>A	NP_620594.1:p.Arg954=
NM_139026.6:c.2767C>A	NP_620595.1:p.Arg923=
NM_139027.6:c.2860C>A MANE Select	NP_620596.2:p.Arg954=
NR_024514.3:n.1697C>A