Canonical Allele Identifier: CA375410000

Gene: ADAMTS13

Linked Data

• MyVariant Identifiers: chr9:g.133454428T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133454428T>G , CM000671.2:g.133454428T>G	GRCh38
NC_000009.10:g.135309371T>G	NCBI36
NG_011934.2:g.45090T>G , LRG_544:g.45090T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355699.7:c.3058T>G MANE Select	ENSP00000347927.2:p.Ser1020Ala
ENST00000355699.6:c.3058T>G	ENSP00000347927.2:p.Ser1020Ala
ENST00000356589.6:c.2965T>G	ENSP00000348997.2:p.Ser989Ala
ENST00000371916.5:c.*527T>G	ENSP00000360984.2:n.*527T>G
ENST00000371929.7:c.3058T>G	ENSP00000360997.3:p.Ser1020Ala
ENST00000485925.5:n.1874T>G
NM_139025.4:c.3058T>G , LRG_544t1:c.3058T>G	NP_620594.1:p.Ser1020Ala
NM_139026.4:c.2965T>G	NP_620595.1:p.Ser989Ala
NM_139027.4:c.3058T>G	NP_620596.2:p.Ser1020Ala
NR_024514.2:n.1893T>G
XM_011518174.1:c.2668T>G	XP_011516476.1:p.Ser890Ala
XM_011518175.1:c.3058T>G	XP_011516477.1:p.Ser1020Ala
XM_011518176.1:c.2074T>G	XP_011516478.1:p.Ser692Ala
XM_011518177.1:c.2068T>G	XP_011516479.1:p.Ser690Ala
XM_011518178.1:c.1723T>G	XP_011516480.1:p.Ser575Ala
XM_011518179.1:c.1723T>G	XP_011516481.1:p.Ser575Ala
XM_011518180.1:c.1324T>G	XP_011516482.1:p.Ser442Ala
XM_011518176.3:c.2074T>G	XP_011516478.1:p.Ser692Ala
XM_011518178.2:c.1723T>G	XP_011516480.1:p.Ser575Ala
XM_017014232.1:c.3046T>G	XP_016869721.1:p.Ser1016Ala
XM_017014233.1:c.2668T>G	XP_016869722.1:p.Ser890Ala
XM_017014234.2:c.2068T>G	XP_016869723.1:p.Ser690Ala
XR_001746171.1:n.3831T>G
NM_139026.5:c.2965T>G	NP_620595.1:p.Ser989Ala
NM_139027.5:c.3058T>G	NP_620596.2:p.Ser1020Ala
NM_139025.5:c.3058T>G	NP_620594.1:p.Ser1020Ala
NM_139026.6:c.2965T>G	NP_620595.1:p.Ser989Ala
NM_139027.6:c.3058T>G MANE Select	NP_620596.2:p.Ser1020Ala
NR_024514.3:n.1895T>G