Canonical Allele Identifier: CA375410572

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454525A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454525A>T , CM000671.2:g.133454525A>T	GRCh38
NC_000009.10:g.135309468A>T	NCBI36
NG_011934.2:g.45187A>T , LRG_544:g.45187A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3155A>T MANE Select	ENSP00000347927.2:p.Glu1052Val
ENST00000355699.6:c.3155A>T	ENSP00000347927.2:p.Glu1052Val
ENST00000356589.6:c.3062A>T	ENSP00000348997.2:p.Glu1021Val
ENST00000371916.5:c.*624A>T	ENSP00000360984.2:n.*624A>T
ENST00000371929.7:c.3155A>T	ENSP00000360997.3:p.Glu1052Val
ENST00000485925.5:n.1971A>T
NM_139025.4:c.3155A>T , LRG_544t1:c.3155A>T	NP_620594.1:p.Glu1052Val
NM_139026.4:c.3062A>T	NP_620595.1:p.Glu1021Val
NM_139027.4:c.3155A>T	NP_620596.2:p.Glu1052Val
NR_024514.2:n.1990A>T
XM_011518174.1:c.2765A>T	XP_011516476.1:p.Glu922Val
XM_011518175.1:c.3155A>T	XP_011516477.1:p.Glu1052Val
XM_011518176.1:c.2171A>T	XP_011516478.1:p.Glu724Val
XM_011518177.1:c.2165A>T	XP_011516479.1:p.Glu722Val
XM_011518178.1:c.1820A>T	XP_011516480.1:p.Glu607Val
XM_011518179.1:c.1820A>T	XP_011516481.1:p.Glu607Val
XM_011518180.1:c.1421A>T	XP_011516482.1:p.Glu474Val
XM_011518176.3:c.2171A>T	XP_011516478.1:p.Glu724Val
XM_011518178.2:c.1820A>T	XP_011516480.1:p.Glu607Val
XM_017014232.1:c.3143A>T	XP_016869721.1:p.Glu1048Val
XM_017014233.1:c.2765A>T	XP_016869722.1:p.Glu922Val
XM_017014234.2:c.2165A>T	XP_016869723.1:p.Glu722Val
NM_139026.5:c.3062A>T	NP_620595.1:p.Glu1021Val
NM_139027.5:c.3155A>T	NP_620596.2:p.Glu1052Val
NM_139025.5:c.3155A>T	NP_620594.1:p.Glu1052Val
NM_139026.6:c.3062A>T	NP_620595.1:p.Glu1021Val
NM_139027.6:c.3155A>T MANE Select	NP_620596.2:p.Glu1052Val
NR_024514.3:n.1992A>T