Canonical Allele Identifier: CA375391591

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133436872C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436872C>A , CM000671.2:g.133436872C>A	GRCh38
NC_000009.10:g.135291813C>A	NCBI36
NG_011934.2:g.27534C>A , LRG_544:g.27534C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355699.7:c.1352C>A MANE Select	ENSP00000347927.2:p.Ala451Asp
ENST00000355699.6:c.1352C>A	ENSP00000347927.2:p.Ala451Asp
ENST00000356589.6:c.1259C>A	ENSP00000348997.2:p.Ala420Asp
ENST00000371916.5:c.608C>A	ENSP00000360984.2:p.Ala203Asp
ENST00000371929.7:c.1352C>A	ENSP00000360997.3:p.Ala451Asp
ENST00000474918.1:c.*156C>A	ENSP00000435305.1:n.*156C>A
ENST00000485925.5:n.974-2494C>A
ENST00000495234.5:c.*636C>A	ENSP00000435274.1:n.*636C>A
NM_139025.4:c.1352C>A , LRG_544t1:c.1352C>A	NP_620594.1:p.Ala451Asp
NM_139026.4:c.1259C>A	NP_620595.1:p.Ala420Asp
NM_139027.4:c.1352C>A	NP_620596.2:p.Ala451Asp
NR_024514.2:n.993-2494C>A
XM_011518174.1:c.962C>A	XP_011516476.1:p.Ala321Asp
XM_011518175.1:c.1352C>A	XP_011516477.1:p.Ala451Asp
XM_011518176.1:c.368C>A	XP_011516478.1:p.Ala123Asp
XM_011518177.1:c.362C>A	XP_011516479.1:p.Ala121Asp
XM_011518178.1:c.17C>A	XP_011516480.1:p.Ala6Asp
XM_011518179.1:c.138C>A	XP_011516481.1:p.Arg46=
XM_011518180.1:c.687-7991C>A	XP_011516482.1:n.687-7991C>A
XM_011518176.3:c.368C>A	XP_011516478.1:p.Ala123Asp
XM_011518178.2:c.17C>A	XP_011516480.1:p.Ala6Asp
XM_017014232.1:c.1340C>A	XP_016869721.1:p.Ala447Asp
XM_017014233.1:c.962C>A	XP_016869722.1:p.Ala321Asp
XM_017014234.2:c.362C>A	XP_016869723.1:p.Ala121Asp
XM_017014235.1:c.1352C>A	XP_016869724.1:p.Ala451Asp
XR_001746171.1:n.2577C>A
NM_139026.5:c.1259C>A	NP_620595.1:p.Ala420Asp
NM_139027.5:c.1352C>A	NP_620596.2:p.Ala451Asp
NM_139025.5:c.1352C>A	NP_620594.1:p.Ala451Asp
NM_139026.6:c.1259C>A	NP_620595.1:p.Ala420Asp
NM_139027.6:c.1352C>A MANE Select	NP_620596.2:p.Ala451Asp
NR_024514.3:n.995-2494C>A