Canonical Allele Identifier: CA375397836

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133443524-G-A
• MyVariant Identifiers: chr9:g.133443524G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133443524G>A , CM000671.2:g.133443524G>A	GRCh38
NC_000009.10:g.135298466G>A	NCBI36
NG_011934.2:g.34186G>A , LRG_544:g.34186G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.2383G>A MANE Select	ENSP00000347927.2:p.Ala795Thr
ENST00000355699.6:c.2383G>A	ENSP00000347927.2:p.Ala795Thr
ENST00000356589.6:c.2290G>A	ENSP00000348997.2:p.Ala764Thr
ENST00000371916.5:c.1225-1339G>A	ENSP00000360984.2:n.1225-1339G>A
ENST00000371929.7:c.2383G>A	ENSP00000360997.3:p.Ala795Thr
ENST00000474918.1:c.*921G>A	ENSP00000435305.1:n.*921G>A
ENST00000485925.5:n.1237-1339G>A
ENST00000495234.5:c.*1253-1339G>A	ENSP00000435274.1:n.*1253-1339G>A
NM_139025.4:c.2383G>A , LRG_544t1:c.2383G>A	NP_620594.1:p.Ala795Thr
NM_139026.4:c.2290G>A	NP_620595.1:p.Ala764Thr
NM_139027.4:c.2383G>A	NP_620596.2:p.Ala795Thr
NR_024514.2:n.1256-1339G>A
XM_011518174.1:c.1993G>A	XP_011516476.1:p.Ala665Thr
XM_011518175.1:c.2383G>A	XP_011516477.1:p.Ala795Thr
XM_011518176.1:c.1399G>A	XP_011516478.1:p.Ala467Thr
XM_011518177.1:c.1393G>A	XP_011516479.1:p.Ala465Thr
XM_011518178.1:c.1048G>A	XP_011516480.1:p.Ala350Thr
XM_011518179.1:c.1048G>A	XP_011516481.1:p.Ala350Thr
XM_011518180.1:c.687-1339G>A	XP_011516482.1:n.687-1339G>A
XM_011518176.3:c.1399G>A	XP_011516478.1:p.Ala467Thr
XM_011518178.2:c.1048G>A	XP_011516480.1:p.Ala350Thr
XM_017014232.1:c.2371G>A	XP_016869721.1:p.Ala791Thr
XM_017014233.1:c.1993G>A	XP_016869722.1:p.Ala665Thr
XM_017014234.2:c.1393G>A	XP_016869723.1:p.Ala465Thr
XM_017014235.1:c.2234+781G>A	XP_016869724.1:n.2234+781G>A
XR_001746171.1:n.3194-1339G>A
NM_139026.5:c.2290G>A	NP_620595.1:p.Ala764Thr
NM_139027.5:c.2383G>A	NP_620596.2:p.Ala795Thr
NM_139025.5:c.2383G>A	NP_620594.1:p.Ala795Thr
NM_139026.6:c.2290G>A	NP_620595.1:p.Ala764Thr
NM_139027.6:c.2383G>A MANE Select	NP_620596.2:p.Ala795Thr
NR_024514.3:n.1258-1339G>A