Canonical Allele Identifier: CA375391668

Gene: ADAMTS13

Linked Data

• gnomAD v4: 9-133436890-C-A
• MyVariant Identifiers: chr9:g.133436890C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436890C>A , CM000671.2:g.133436890C>A	GRCh38
NC_000009.10:g.135291831C>A	NCBI36
NG_011934.2:g.27552C>A , LRG_544:g.27552C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1370C>A MANE Select	ENSP00000347927.2:p.Pro457Gln
ENST00000355699.6:c.1370C>A	ENSP00000347927.2:p.Pro457Gln
ENST00000356589.6:c.1277C>A	ENSP00000348997.2:p.Pro426Gln
ENST00000371916.5:c.626C>A	ENSP00000360984.2:p.Pro209Gln
ENST00000371929.7:c.1370C>A	ENSP00000360997.3:p.Pro457Gln
ENST00000474918.1:c.*174C>A	ENSP00000435305.1:n.*174C>A
ENST00000485925.5:n.974-2476C>A
ENST00000495234.5:c.*654C>A	ENSP00000435274.1:n.*654C>A
NM_139025.4:c.1370C>A , LRG_544t1:c.1370C>A	NP_620594.1:p.Pro457Gln
NM_139026.4:c.1277C>A	NP_620595.1:p.Pro426Gln
NM_139027.4:c.1370C>A	NP_620596.2:p.Pro457Gln
NR_024514.2:n.993-2476C>A
XM_011518174.1:c.980C>A	XP_011516476.1:p.Pro327Gln
XM_011518175.1:c.1370C>A	XP_011516477.1:p.Pro457Gln
XM_011518176.1:c.386C>A	XP_011516478.1:p.Pro129Gln
XM_011518177.1:c.380C>A	XP_011516479.1:p.Pro127Gln
XM_011518178.1:c.35C>A	XP_011516480.1:p.Pro12Gln
XM_011518179.1:c.156C>A	XP_011516481.1:p.Ala52=
XM_011518180.1:c.687-7973C>A	XP_011516482.1:n.687-7973C>A
XM_011518176.3:c.386C>A	XP_011516478.1:p.Pro129Gln
XM_011518178.2:c.35C>A	XP_011516480.1:p.Pro12Gln
XM_017014232.1:c.1358C>A	XP_016869721.1:p.Pro453Gln
XM_017014233.1:c.980C>A	XP_016869722.1:p.Pro327Gln
XM_017014234.2:c.380C>A	XP_016869723.1:p.Pro127Gln
XM_017014235.1:c.1370C>A	XP_016869724.1:p.Pro457Gln
XR_001746171.1:n.2595C>A
NM_139026.5:c.1277C>A	NP_620595.1:p.Pro426Gln
NM_139027.5:c.1370C>A	NP_620596.2:p.Pro457Gln
NM_139025.5:c.1370C>A	NP_620594.1:p.Pro457Gln
NM_139026.6:c.1277C>A	NP_620595.1:p.Pro426Gln
NM_139027.6:c.1370C>A MANE Select	NP_620596.2:p.Pro457Gln
NR_024514.3:n.995-2476C>A