Canonical Allele Identifier: CA375414828

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133456093A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133456093A>T , CM000671.2:g.133456093A>T	GRCh38
NC_000009.10:g.135311036A>T	NCBI36
NG_011934.2:g.46755A>T , LRG_544:g.46755A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3425A>T MANE Select	ENSP00000347927.2:p.Glu1142Val
ENST00000355699.6:c.3425A>T	ENSP00000347927.2:p.Glu1142Val
ENST00000356589.6:c.3332A>T	ENSP00000348997.2:p.Glu1111Val
ENST00000371910.1:c.-20A>T	ENSP00000360978.1:n.-20A>T
ENST00000371916.5:c.*894A>T	ENSP00000360984.2:n.*894A>T
ENST00000371929.7:c.3593A>T	ENSP00000360997.3:p.Glu1198Val
ENST00000485925.5:n.2241A>T
NM_139025.4:c.3593A>T , LRG_544t1:c.3593A>T	NP_620594.1:p.Glu1198Val
NM_139026.4:c.3332A>T	NP_620595.1:p.Glu1111Val
NM_139027.4:c.3425A>T	NP_620596.2:p.Glu1142Val
NR_024514.2:n.2260A>T
XM_011518174.1:c.3203A>T	XP_011516476.1:p.Glu1068Val
XM_011518175.1:c.3594A>T	XP_011516477.1:p.Ter1198Cys
XM_011518176.1:c.2609A>T	XP_011516478.1:p.Glu870Val
XM_011518177.1:c.2603A>T	XP_011516479.1:p.Glu868Val
XM_011518178.1:c.2258A>T	XP_011516480.1:p.Glu753Val
XM_011518179.1:c.2258A>T	XP_011516481.1:p.Glu753Val
XM_011518180.1:c.1859A>T	XP_011516482.1:p.Glu620Val
XM_011518176.3:c.2609A>T	XP_011516478.1:p.Glu870Val
XM_011518178.2:c.2258A>T	XP_011516480.1:p.Glu753Val
XM_017014232.1:c.3581A>T	XP_016869721.1:p.Glu1194Val
XM_017014233.1:c.3203A>T	XP_016869722.1:p.Glu1068Val
XM_017014234.2:c.2603A>T	XP_016869723.1:p.Glu868Val
NM_139026.5:c.3332A>T	NP_620595.1:p.Glu1111Val
NM_139027.5:c.3425A>T	NP_620596.2:p.Glu1142Val
NM_139025.5:c.3593A>T	NP_620594.1:p.Glu1198Val
NM_139026.6:c.3332A>T	NP_620595.1:p.Glu1111Val
NM_139027.6:c.3425A>T MANE Select	NP_620596.2:p.Glu1142Val
NR_024514.3:n.2262A>T