Canonical Allele Identifier: CA375410631

Gene: ADAMTS13

Linked Data

• dbSNP Id: rs1842626920
• MyVariant Identifiers: chr9:g.133454535T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454535T>G , CM000671.2:g.133454535T>G	GRCh38
NC_000009.10:g.135309478T>G	NCBI36
NG_011934.2:g.45197T>G , LRG_544:g.45197T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3165T>G MANE Select	ENSP00000347927.2:p.Cys1055Trp
ENST00000355699.6:c.3165T>G	ENSP00000347927.2:p.Cys1055Trp
ENST00000356589.6:c.3072T>G	ENSP00000348997.2:p.Cys1024Trp
ENST00000371916.5:c.*634T>G	ENSP00000360984.2:n.*634T>G
ENST00000371929.7:c.3165T>G	ENSP00000360997.3:p.Cys1055Trp
ENST00000485925.5:n.1981T>G
NM_139025.4:c.3165T>G , LRG_544t1:c.3165T>G	NP_620594.1:p.Cys1055Trp
NM_139026.4:c.3072T>G	NP_620595.1:p.Cys1024Trp
NM_139027.4:c.3165T>G	NP_620596.2:p.Cys1055Trp
NR_024514.2:n.2000T>G
XM_011518174.1:c.2775T>G	XP_011516476.1:p.Cys925Trp
XM_011518175.1:c.3165T>G	XP_011516477.1:p.Cys1055Trp
XM_011518176.1:c.2181T>G	XP_011516478.1:p.Cys727Trp
XM_011518177.1:c.2175T>G	XP_011516479.1:p.Cys725Trp
XM_011518178.1:c.1830T>G	XP_011516480.1:p.Cys610Trp
XM_011518179.1:c.1830T>G	XP_011516481.1:p.Cys610Trp
XM_011518180.1:c.1431T>G	XP_011516482.1:p.Cys477Trp
XM_011518176.3:c.2181T>G	XP_011516478.1:p.Cys727Trp
XM_011518178.2:c.1830T>G	XP_011516480.1:p.Cys610Trp
XM_017014232.1:c.3153T>G	XP_016869721.1:p.Cys1051Trp
XM_017014233.1:c.2775T>G	XP_016869722.1:p.Cys925Trp
XM_017014234.2:c.2175T>G	XP_016869723.1:p.Cys725Trp
NM_139026.5:c.3072T>G	NP_620595.1:p.Cys1024Trp
NM_139027.5:c.3165T>G	NP_620596.2:p.Cys1055Trp
NM_139025.5:c.3165T>G	NP_620594.1:p.Cys1055Trp
NM_139026.6:c.3072T>G	NP_620595.1:p.Cys1024Trp
NM_139027.6:c.3165T>G MANE Select	NP_620596.2:p.Cys1055Trp
NR_024514.3:n.2002T>G