Canonical Allele Identifier: CA375391619

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133436878C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133436878C>G , CM000671.2:g.133436878C>G	GRCh38
NC_000009.10:g.135291819C>G	NCBI36
NG_011934.2:g.27540C>G , LRG_544:g.27540C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.1358C>G MANE Select	ENSP00000347927.2:p.Thr453Ser
ENST00000355699.6:c.1358C>G	ENSP00000347927.2:p.Thr453Ser
ENST00000356589.6:c.1265C>G	ENSP00000348997.2:p.Thr422Ser
ENST00000371916.5:c.614C>G	ENSP00000360984.2:p.Thr205Ser
ENST00000371929.7:c.1358C>G	ENSP00000360997.3:p.Thr453Ser
ENST00000474918.1:c.*162C>G	ENSP00000435305.1:n.*162C>G
ENST00000485925.5:n.974-2488C>G
ENST00000495234.5:c.*642C>G	ENSP00000435274.1:n.*642C>G
NM_139025.4:c.1358C>G , LRG_544t1:c.1358C>G	NP_620594.1:p.Thr453Ser
NM_139026.4:c.1265C>G	NP_620595.1:p.Thr422Ser
NM_139027.4:c.1358C>G	NP_620596.2:p.Thr453Ser
NR_024514.2:n.993-2488C>G
XM_011518174.1:c.968C>G	XP_011516476.1:p.Thr323Ser
XM_011518175.1:c.1358C>G	XP_011516477.1:p.Thr453Ser
XM_011518176.1:c.374C>G	XP_011516478.1:p.Thr125Ser
XM_011518177.1:c.368C>G	XP_011516479.1:p.Thr123Ser
XM_011518178.1:c.23C>G	XP_011516480.1:p.Thr8Ser
XM_011518179.1:c.144C>G	XP_011516481.1:p.Asp48Glu
XM_011518180.1:c.687-7985C>G	XP_011516482.1:n.687-7985C>G
XM_011518176.3:c.374C>G	XP_011516478.1:p.Thr125Ser
XM_011518178.2:c.23C>G	XP_011516480.1:p.Thr8Ser
XM_017014232.1:c.1346C>G	XP_016869721.1:p.Thr449Ser
XM_017014233.1:c.968C>G	XP_016869722.1:p.Thr323Ser
XM_017014234.2:c.368C>G	XP_016869723.1:p.Thr123Ser
XM_017014235.1:c.1358C>G	XP_016869724.1:p.Thr453Ser
XR_001746171.1:n.2583C>G
NM_139026.5:c.1265C>G	NP_620595.1:p.Thr422Ser
NM_139027.5:c.1358C>G	NP_620596.2:p.Thr453Ser
NM_139025.5:c.1358C>G	NP_620594.1:p.Thr453Ser
NM_139026.6:c.1265C>G	NP_620595.1:p.Thr422Ser
NM_139027.6:c.1358C>G MANE Select	NP_620596.2:p.Thr453Ser
NR_024514.3:n.995-2488C>G