Canonical Allele Identifier: CA200939951

Gene: ADAMTS13

Linked Data

• dbSNP Id: rs368433734
• MyVariant Identifiers: chr9:g.133449800C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133449800C>A , CM000671.2:g.133449800C>A	GRCh38
NC_000009.10:g.135304742C>A	NCBI36
NG_011934.2:g.40462C>A , LRG_544:g.40462C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2879C>A MANE Select	ENSP00000347927.2:p.Ala960Glu
ENST00000355699.6:c.2879C>A	ENSP00000347927.2:p.Ala960Glu
ENST00000356589.6:c.2786C>A	ENSP00000348997.2:p.Ala929Glu
ENST00000371916.5:c.*348C>A	ENSP00000360984.2:n.*348C>A
ENST00000371929.7:c.2879C>A	ENSP00000360997.3:p.Ala960Glu
ENST00000485925.5:n.1695C>A
ENST00000495234.5:c.*1711C>A	ENSP00000435274.1:n.*1711C>A
NM_139025.4:c.2879C>A , LRG_544t1:c.2879C>A	NP_620594.1:p.Ala960Glu
NM_139026.4:c.2786C>A	NP_620595.1:p.Ala929Glu
NM_139027.4:c.2879C>A	NP_620596.2:p.Ala960Glu
NR_024514.2:n.1714C>A
XM_011518174.1:c.2489C>A	XP_011516476.1:p.Ala830Glu
XM_011518175.1:c.2879C>A	XP_011516477.1:p.Ala960Glu
XM_011518176.1:c.1895C>A	XP_011516478.1:p.Ala632Glu
XM_011518177.1:c.1889C>A	XP_011516479.1:p.Ala630Glu
XM_011518178.1:c.1544C>A	XP_011516480.1:p.Ala515Glu
XM_011518179.1:c.1544C>A	XP_011516481.1:p.Ala515Glu
XM_011518180.1:c.1145C>A	XP_011516482.1:p.Ala382Glu
XM_011518176.3:c.1895C>A	XP_011516478.1:p.Ala632Glu
XM_011518178.2:c.1544C>A	XP_011516480.1:p.Ala515Glu
XM_017014232.1:c.2867C>A	XP_016869721.1:p.Ala956Glu
XM_017014233.1:c.2489C>A	XP_016869722.1:p.Ala830Glu
XM_017014234.2:c.1889C>A	XP_016869723.1:p.Ala630Glu
XR_001746171.1:n.3652C>A
NM_139026.5:c.2786C>A	NP_620595.1:p.Ala929Glu
NM_139027.5:c.2879C>A	NP_620596.2:p.Ala960Glu
NM_139025.5:c.2879C>A	NP_620594.1:p.Ala960Glu
NM_139026.6:c.2786C>A	NP_620595.1:p.Ala929Glu
NM_139027.6:c.2879C>A MANE Select	NP_620596.2:p.Ala960Glu
NR_024514.3:n.1716C>A