Canonical Allele Identifier: CA375409964

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454423T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454423T>A , CM000671.2:g.133454423T>A	GRCh38
NC_000009.10:g.135309366T>A	NCBI36
NG_011934.2:g.45085T>A , LRG_544:g.45085T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3053T>A MANE Select	ENSP00000347927.2:p.Val1018Asp
ENST00000355699.6:c.3053T>A	ENSP00000347927.2:p.Val1018Asp
ENST00000356589.6:c.2960T>A	ENSP00000348997.2:p.Val987Asp
ENST00000371916.5:c.*522T>A	ENSP00000360984.2:n.*522T>A
ENST00000371929.7:c.3053T>A	ENSP00000360997.3:p.Val1018Asp
ENST00000485925.5:n.1869T>A
NM_139025.4:c.3053T>A , LRG_544t1:c.3053T>A	NP_620594.1:p.Val1018Asp
NM_139026.4:c.2960T>A	NP_620595.1:p.Val987Asp
NM_139027.4:c.3053T>A	NP_620596.2:p.Val1018Asp
NR_024514.2:n.1888T>A
XM_011518174.1:c.2663T>A	XP_011516476.1:p.Val888Asp
XM_011518175.1:c.3053T>A	XP_011516477.1:p.Val1018Asp
XM_011518176.1:c.2069T>A	XP_011516478.1:p.Val690Asp
XM_011518177.1:c.2063T>A	XP_011516479.1:p.Val688Asp
XM_011518178.1:c.1718T>A	XP_011516480.1:p.Val573Asp
XM_011518179.1:c.1718T>A	XP_011516481.1:p.Val573Asp
XM_011518180.1:c.1319T>A	XP_011516482.1:p.Val440Asp
XM_011518176.3:c.2069T>A	XP_011516478.1:p.Val690Asp
XM_011518178.2:c.1718T>A	XP_011516480.1:p.Val573Asp
XM_017014232.1:c.3041T>A	XP_016869721.1:p.Val1014Asp
XM_017014233.1:c.2663T>A	XP_016869722.1:p.Val888Asp
XM_017014234.2:c.2063T>A	XP_016869723.1:p.Val688Asp
XR_001746171.1:n.3826T>A
NM_139026.5:c.2960T>A	NP_620595.1:p.Val987Asp
NM_139027.5:c.3053T>A	NP_620596.2:p.Val1018Asp
NM_139025.5:c.3053T>A	NP_620594.1:p.Val1018Asp
NM_139026.6:c.2960T>A	NP_620595.1:p.Val987Asp
NM_139027.6:c.3053T>A MANE Select	NP_620596.2:p.Val1018Asp
NR_024514.3:n.1890T>A