Canonical Allele Identifier: CA200934777
Gene: ADAMTS13 HGNC NCBI

Linked Data

dbSNP Id: rs782729939
MyVariant Identifiers: chr9:g.133443419G>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133443419G>A , CM000671.2:g.133443419G>A GRCh38
NC_000009.10:g.135298361G>A NCBI36
NG_011934.2:g.34081G>A , LRG_544:g.34081G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355699.7:c.2278G>A MANE Select ENSP00000347927.2:p.Gly760Ser
ENST00000355699.6:c.2278G>A ENSP00000347927.2:p.Gly760Ser
ENST00000356589.6:c.2185G>A ENSP00000348997.2:p.Gly729Ser
ENST00000371916.5:c.1225-1444G>A ENSP00000360984.2:n.1225-1444G>A
ENST00000371929.7:c.2278G>A ENSP00000360997.3:p.Gly760Ser
ENST00000474918.1:c.*816G>A ENSP00000435305.1:n.*816G>A
ENST00000485925.5:n.1237-1444G>A
ENST00000495234.5:c.*1253-1444G>A ENSP00000435274.1:n.*1253-1444G>A
NM_139025.4:c.2278G>A , LRG_544t1:c.2278G>A NP_620594.1:p.Gly760Ser
NM_139026.4:c.2185G>A NP_620595.1:p.Gly729Ser
NM_139027.4:c.2278G>A NP_620596.2:p.Gly760Ser
NR_024514.2:n.1256-1444G>A
XM_011518174.1:c.1888G>A XP_011516476.1:p.Gly630Ser
XM_011518175.1:c.2278G>A XP_011516477.1:p.Gly760Ser
XM_011518176.1:c.1294G>A XP_011516478.1:p.Gly432Ser
XM_011518177.1:c.1288G>A XP_011516479.1:p.Gly430Ser
XM_011518178.1:c.943G>A XP_011516480.1:p.Gly315Ser
XM_011518179.1:c.943G>A XP_011516481.1:p.Gly315Ser
XM_011518180.1:c.687-1444G>A XP_011516482.1:n.687-1444G>A
XM_011518176.3:c.1294G>A XP_011516478.1:p.Gly432Ser
XM_011518178.2:c.943G>A XP_011516480.1:p.Gly315Ser
XM_017014232.1:c.2266G>A XP_016869721.1:p.Gly756Ser
XM_017014233.1:c.1888G>A XP_016869722.1:p.Gly630Ser
XM_017014234.2:c.1288G>A XP_016869723.1:p.Gly430Ser
XM_017014235.1:c.2234+676G>A XP_016869724.1:n.2234+676G>A
XR_001746171.1:n.3194-1444G>A
NM_139026.5:c.2185G>A NP_620595.1:p.Gly729Ser
NM_139027.5:c.2278G>A NP_620596.2:p.Gly760Ser
NM_139025.5:c.2278G>A NP_620594.1:p.Gly760Ser
NM_139026.6:c.2185G>A NP_620595.1:p.Gly729Ser
NM_139027.6:c.2278G>A MANE Select NP_620596.2:p.Gly760Ser
NR_024514.3:n.1258-1444G>A