Canonical Allele Identifier: CA860755453

Gene: ADAMTS13

Linked Data

• dbSNP Id: rs1554789140
• MyVariant Identifiers: chr9:g.133436822_133436824del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436822_133436824del , CM000671.2:g.133436822_133436824del	GRCh38
NC_000009.10:g.135291763_135291765del	NCBI36
NG_011934.2:g.27484_27486del , LRG_544:g.27484_27486del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1309-7_1309-5del MANE Select	ENSP00000347927.2:n.1309-7_1309-5del
ENST00000355699.6:c.1309-7_1309-5del	ENSP00000347927.2:n.1309-7_1309-5del
ENST00000356589.6:c.1216-7_1216-5del	ENSP00000348997.2:n.1216-7_1216-5del
ENST00000371916.5:c.565-7_565-5del	ENSP00000360984.2:n.565-7_565-5del
ENST00000371929.7:c.1309-7_1309-5del	ENSP00000360997.3:n.1309-7_1309-5del
ENST00000474918.1:c.*113-7_*113-5del	ENSP00000435305.1:n.*113-7_*113-5del
ENST00000485925.5:n.974-2544_974-2542del
ENST00000495234.5:c.*593-7_*593-5del	ENSP00000435274.1:n.*593-7_*593-5del
NM_139025.4:c.1309-7_1309-5del , LRG_544t1:c.1309-7_1309-5del	NP_620594.1:n.1309-7_1309-5del
NM_139026.4:c.1216-7_1216-5del	NP_620595.1:n.1216-7_1216-5del
NM_139027.4:c.1309-7_1309-5del	NP_620596.2:n.1309-7_1309-5del
NR_024514.2:n.993-2544_993-2542del
XM_011518174.1:c.919-7_919-5del	XP_011516476.1:n.919-7_919-5del
XM_011518175.1:c.1309-7_1309-5del	XP_011516477.1:n.1309-7_1309-5del
XM_011518176.1:c.325-7_325-5del	XP_011516478.1:n.325-7_325-5del
XM_011518177.1:c.319-7_319-5del	XP_011516479.1:n.319-7_319-5del
XM_011518178.1:c.-27-7_-27-5del	XP_011516480.1:n.-27-7_-27-5del
XM_011518179.1:c.95-7_95-5del	XP_011516481.1:n.95-7_95-5del
XM_011518180.1:c.687-8041_687-8039del	XP_011516482.1:n.687-8041_687-8039del
XM_011518176.3:c.325-7_325-5del	XP_011516478.1:n.325-7_325-5del
XM_011518178.2:c.-27-7_-27-5del	XP_011516480.1:n.-27-7_-27-5del
XM_017014232.1:c.1297-7_1297-5del	XP_016869721.1:n.1297-7_1297-5del
XM_017014233.1:c.919-7_919-5del	XP_016869722.1:n.919-7_919-5del
XM_017014234.2:c.319-7_319-5del	XP_016869723.1:n.319-7_319-5del
XM_017014235.1:c.1309-7_1309-5del	XP_016869724.1:n.1309-7_1309-5del
XR_001746171.1:n.2534-7_2534-5del
NM_139026.5:c.1216-7_1216-5del	NP_620595.1:n.1216-7_1216-5del
NM_139027.5:c.1309-7_1309-5del	NP_620596.2:n.1309-7_1309-5del
NM_139025.5:c.1309-7_1309-5del	NP_620594.1:n.1309-7_1309-5del
NM_139026.6:c.1216-7_1216-5del	NP_620595.1:n.1216-7_1216-5del
NM_139027.6:c.1309-7_1309-5del MANE Select	NP_620596.2:n.1309-7_1309-5del
NR_024514.3:n.995-2544_995-2542del