Canonical Allele Identifier: CA375391791

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133436922T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436922T>G , CM000671.2:g.133436922T>G	GRCh38
NC_000009.10:g.135291863T>G	NCBI36
NG_011934.2:g.27584T>G , LRG_544:g.27584T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1402T>G MANE Select	ENSP00000347927.2:p.Tyr468Asp
ENST00000355699.6:c.1402T>G	ENSP00000347927.2:p.Tyr468Asp
ENST00000356589.6:c.1309T>G	ENSP00000348997.2:p.Tyr437Asp
ENST00000371916.5:c.658T>G	ENSP00000360984.2:p.Tyr220Asp
ENST00000371929.7:c.1402T>G	ENSP00000360997.3:p.Tyr468Asp
ENST00000474918.1:c.*206T>G	ENSP00000435305.1:n.*206T>G
ENST00000485925.5:n.974-2444T>G
ENST00000495234.5:c.*686T>G	ENSP00000435274.1:n.*686T>G
NM_139025.4:c.1402T>G , LRG_544t1:c.1402T>G	NP_620594.1:p.Tyr468Asp
NM_139026.4:c.1309T>G	NP_620595.1:p.Tyr437Asp
NM_139027.4:c.1402T>G	NP_620596.2:p.Tyr468Asp
NR_024514.2:n.993-2444T>G
XM_011518174.1:c.1012T>G	XP_011516476.1:p.Tyr338Asp
XM_011518175.1:c.1402T>G	XP_011516477.1:p.Tyr468Asp
XM_011518176.1:c.418T>G	XP_011516478.1:p.Tyr140Asp
XM_011518177.1:c.412T>G	XP_011516479.1:p.Tyr138Asp
XM_011518178.1:c.67T>G	XP_011516480.1:p.Tyr23Asp
XM_011518179.1:c.188T>G	XP_011516481.1:p.Leu63Arg
XM_011518180.1:c.687-7941T>G	XP_011516482.1:n.687-7941T>G
XM_011518176.3:c.418T>G	XP_011516478.1:p.Tyr140Asp
XM_011518178.2:c.67T>G	XP_011516480.1:p.Tyr23Asp
XM_017014232.1:c.1390T>G	XP_016869721.1:p.Tyr464Asp
XM_017014233.1:c.1012T>G	XP_016869722.1:p.Tyr338Asp
XM_017014234.2:c.412T>G	XP_016869723.1:p.Tyr138Asp
XM_017014235.1:c.1402T>G	XP_016869724.1:p.Tyr468Asp
XR_001746171.1:n.2627T>G
NM_139026.5:c.1309T>G	NP_620595.1:p.Tyr437Asp
NM_139027.5:c.1402T>G	NP_620596.2:p.Tyr468Asp
NM_139025.5:c.1402T>G	NP_620594.1:p.Tyr468Asp
NM_139026.6:c.1309T>G	NP_620595.1:p.Tyr437Asp
NM_139027.6:c.1402T>G MANE Select	NP_620596.2:p.Tyr468Asp
NR_024514.3:n.995-2444T>G