Canonical Allele Identifier: CA2838915351

Gene: ADAMTS13

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133448723T>A , CM000671.2:g.133448723T>A	GRCh38
NC_000009.10:g.135303665T>A	NCBI36
NG_011934.2:g.39385T>A , LRG_544:g.39385T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2856T>A MANE Select	ENSP00000347927.2:p.Pro952=
ENST00000355699.6:c.2856T>A	ENSP00000347927.2:p.Pro952=
ENST00000356589.6:c.2763T>A	ENSP00000348997.2:p.Pro921=
ENST00000371916.5:c.*325T>A	ENSP00000360984.2:n.*325T>A
ENST00000371929.7:c.2856T>A	ENSP00000360997.3:p.Pro952=
ENST00000485925.5:n.1672T>A
ENST00000495234.5:c.*1688T>A	ENSP00000435274.1:n.*1688T>A
NM_139025.4:c.2856T>A , LRG_544t1:c.2856T>A	NP_620594.1:p.Pro952=
NM_139026.4:c.2763T>A	NP_620595.1:p.Pro921=
NM_139027.4:c.2856T>A	NP_620596.2:p.Pro952=
NR_024514.2:n.1691T>A
XM_011518174.1:c.2466T>A	XP_011516476.1:p.Pro822=
XM_011518175.1:c.2856T>A	XP_011516477.1:p.Pro952=
XM_011518176.1:c.1872T>A	XP_011516478.1:p.Pro624=
XM_011518177.1:c.1866T>A	XP_011516479.1:p.Pro622=
XM_011518178.1:c.1521T>A	XP_011516480.1:p.Pro507=
XM_011518179.1:c.1521T>A	XP_011516481.1:p.Pro507=
XM_011518180.1:c.1122T>A	XP_011516482.1:p.Pro374=
XM_011518176.3:c.1872T>A	XP_011516478.1:p.Pro624=
XM_011518178.2:c.1521T>A	XP_011516480.1:p.Pro507=
XM_017014232.1:c.2844T>A	XP_016869721.1:p.Pro948=
XM_017014233.1:c.2466T>A	XP_016869722.1:p.Pro822=
XM_017014234.2:c.1866T>A	XP_016869723.1:p.Pro622=
XR_001746171.1:n.3629T>A
NM_139026.5:c.2763T>A	NP_620595.1:p.Pro921=
NM_139027.5:c.2856T>A	NP_620596.2:p.Pro952=
NM_139025.5:c.2856T>A	NP_620594.1:p.Pro952=
NM_139026.6:c.2763T>A	NP_620595.1:p.Pro921=
NM_139027.6:c.2856T>A MANE Select	NP_620596.2:p.Pro952=
NR_024514.3:n.1693T>A