Canonical Allele Identifier: CA375406216
Gene: ADAMTS13 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133449875A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133449875A>G , CM000671.2:g.133449875A>G GRCh38
NC_000009.10:g.135304817A>G NCBI36
NG_011934.2:g.40537A>G , LRG_544:g.40537A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355699.7:c.2954A>G MANE Select ENSP00000347927.2:p.Asp985Gly
ENST00000355699.6:c.2954A>G ENSP00000347927.2:p.Asp985Gly
ENST00000356589.6:c.2861A>G ENSP00000348997.2:p.Asp954Gly
ENST00000371916.5:c.*423A>G ENSP00000360984.2:n.*423A>G
ENST00000371929.7:c.2954A>G ENSP00000360997.3:p.Asp985Gly
ENST00000485925.5:n.1770A>G
ENST00000495234.5:c.*1786A>G ENSP00000435274.1:n.*1786A>G
NM_139025.4:c.2954A>G , LRG_544t1:c.2954A>G NP_620594.1:p.Asp985Gly
NM_139026.4:c.2861A>G NP_620595.1:p.Asp954Gly
NM_139027.4:c.2954A>G NP_620596.2:p.Asp985Gly
NR_024514.2:n.1789A>G
XM_011518174.1:c.2564A>G XP_011516476.1:p.Asp855Gly
XM_011518175.1:c.2954A>G XP_011516477.1:p.Asp985Gly
XM_011518176.1:c.1970A>G XP_011516478.1:p.Asp657Gly
XM_011518177.1:c.1964A>G XP_011516479.1:p.Asp655Gly
XM_011518178.1:c.1619A>G XP_011516480.1:p.Asp540Gly
XM_011518179.1:c.1619A>G XP_011516481.1:p.Asp540Gly
XM_011518180.1:c.1220A>G XP_011516482.1:p.Asp407Gly
XM_011518176.3:c.1970A>G XP_011516478.1:p.Asp657Gly
XM_011518178.2:c.1619A>G XP_011516480.1:p.Asp540Gly
XM_017014232.1:c.2942A>G XP_016869721.1:p.Asp981Gly
XM_017014233.1:c.2564A>G XP_016869722.1:p.Asp855Gly
XM_017014234.2:c.1964A>G XP_016869723.1:p.Asp655Gly
XR_001746171.1:n.3727A>G
NM_139026.5:c.2861A>G NP_620595.1:p.Asp954Gly
NM_139027.5:c.2954A>G NP_620596.2:p.Asp985Gly
NM_139025.5:c.2954A>G NP_620594.1:p.Asp985Gly
NM_139026.6:c.2861A>G NP_620595.1:p.Asp954Gly
NM_139027.6:c.2954A>G MANE Select NP_620596.2:p.Asp985Gly
NR_024514.3:n.1791A>G