Canonical Allele Identifier: CA375410653

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133454540-C-A
• MyVariant Identifiers: chr9:g.133454540C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454540C>A , CM000671.2:g.133454540C>A	GRCh38
NC_000009.10:g.135309483C>A	NCBI36
NG_011934.2:g.45202C>A , LRG_544:g.45202C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3170C>A MANE Select	ENSP00000347927.2:p.Ala1057Glu
ENST00000355699.6:c.3170C>A	ENSP00000347927.2:p.Ala1057Glu
ENST00000356589.6:c.3077C>A	ENSP00000348997.2:p.Ala1026Glu
ENST00000371916.5:c.*639C>A	ENSP00000360984.2:n.*639C>A
ENST00000371929.7:c.3170C>A	ENSP00000360997.3:p.Ala1057Glu
ENST00000485925.5:n.1986C>A
NM_139025.4:c.3170C>A , LRG_544t1:c.3170C>A	NP_620594.1:p.Ala1057Glu
NM_139026.4:c.3077C>A	NP_620595.1:p.Ala1026Glu
NM_139027.4:c.3170C>A	NP_620596.2:p.Ala1057Glu
NR_024514.2:n.2005C>A
XM_011518174.1:c.2780C>A	XP_011516476.1:p.Ala927Glu
XM_011518175.1:c.3170C>A	XP_011516477.1:p.Ala1057Glu
XM_011518176.1:c.2186C>A	XP_011516478.1:p.Ala729Glu
XM_011518177.1:c.2180C>A	XP_011516479.1:p.Ala727Glu
XM_011518178.1:c.1835C>A	XP_011516480.1:p.Ala612Glu
XM_011518179.1:c.1835C>A	XP_011516481.1:p.Ala612Glu
XM_011518180.1:c.1436C>A	XP_011516482.1:p.Ala479Glu
XM_011518176.3:c.2186C>A	XP_011516478.1:p.Ala729Glu
XM_011518178.2:c.1835C>A	XP_011516480.1:p.Ala612Glu
XM_017014232.1:c.3158C>A	XP_016869721.1:p.Ala1053Glu
XM_017014233.1:c.2780C>A	XP_016869722.1:p.Ala927Glu
XM_017014234.2:c.2180C>A	XP_016869723.1:p.Ala727Glu
NM_139026.5:c.3077C>A	NP_620595.1:p.Ala1026Glu
NM_139027.5:c.3170C>A	NP_620596.2:p.Ala1057Glu
NM_139025.5:c.3170C>A	NP_620594.1:p.Ala1057Glu
NM_139026.6:c.3077C>A	NP_620595.1:p.Ala1026Glu
NM_139027.6:c.3170C>A MANE Select	NP_620596.2:p.Ala1057Glu
NR_024514.3:n.2007C>A