Canonical Allele Identifier: CA1882681596
Gene: ADAMTS13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133454444C= , CM000671.2:g.133454444C= GRCh38
NC_000009.10:g.135309387C= NCBI36
NG_011934.2:g.45106C= , LRG_544:g.45106C=

Transcript Alleles

HGVS Amino-acid change
ENST00000355699.7:c.3074C= MANE Select ENSP00000347927.2:p.Ser1025=
ENST00000355699.6:c.3074C= ENSP00000347927.2:p.Ser1025=
ENST00000356589.6:c.2981C= ENSP00000348997.2:p.Ser994=
ENST00000371916.5:c.*543C= ENSP00000360984.2:n.*543C=
ENST00000371929.7:c.3074C= ENSP00000360997.3:p.Ser1025=
ENST00000485925.5:n.1890C=
NM_139025.4:c.3074C= , LRG_544t1:c.3074C= NP_620594.1:p.Ser1025=
NM_139026.4:c.2981C= NP_620595.1:p.Ser994=
NM_139027.4:c.3074C= NP_620596.2:p.Ser1025=
NR_024514.2:n.1909C=
XM_011518174.1:c.2684C= XP_011516476.1:p.Ser895=
XM_011518175.1:c.3074C= XP_011516477.1:p.Ser1025=
XM_011518176.1:c.2090C= XP_011516478.1:p.Ser697=
XM_011518177.1:c.2084C= XP_011516479.1:p.Ser695=
XM_011518178.1:c.1739C= XP_011516480.1:p.Ser580=
XM_011518179.1:c.1739C= XP_011516481.1:p.Ser580=
XM_011518180.1:c.1340C= XP_011516482.1:p.Ser447=
XM_011518176.3:c.2090C= XP_011516478.1:p.Ser697=
XM_011518178.2:c.1739C= XP_011516480.1:p.Ser580=
XM_017014232.1:c.3062C= XP_016869721.1:p.Ser1021=
XM_017014233.1:c.2684C= XP_016869722.1:p.Ser895=
XM_017014234.2:c.2084C= XP_016869723.1:p.Ser695=
XR_001746171.1:n.3847C=
NM_139026.5:c.2981C= NP_620595.1:p.Ser994=
NM_139027.5:c.3074C= NP_620596.2:p.Ser1025=
NM_139025.5:c.3074C= NP_620594.1:p.Ser1025=
NM_139026.6:c.2981C= NP_620595.1:p.Ser994=
NM_139027.6:c.3074C= MANE Select NP_620596.2:p.Ser1025=
NR_024514.3:n.1911C=