Canonical Allele Identifier: CA1882683863
Gene: ADAMTS13 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133459039A= , CM000671.2:g.133459039A= GRCh38
NC_000009.10:g.135313982A= NCBI36
NG_011934.2:g.49701A= , LRG_544:g.49701A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355699.7:c.3975A= MANE Select ENSP00000347927.2:p.Ser1325=
ENST00000355699.6:c.3975A= ENSP00000347927.2:p.Ser1325=
ENST00000356589.6:c.3882A= ENSP00000348997.2:p.Ser1294=
ENST00000371910.1:c.531A= ENSP00000360978.1:p.Ser177=
ENST00000371916.5:c.*1444A= ENSP00000360984.2:n.*1444A=
ENST00000371929.7:c.4143A= ENSP00000360997.3:p.Ser1381=
ENST00000485925.5:n.2606A=
NM_139025.4:c.4143A= , LRG_544t1:c.4143A= NP_620594.1:p.Ser1381=
NM_139026.4:c.3882A= NP_620595.1:p.Ser1294=
NM_139027.4:c.3975A= NP_620596.2:p.Ser1325=
NR_024514.2:n.2625A=
XM_011518174.1:c.3753A= XP_011516476.1:p.Ser1251=
XM_011518176.1:c.3159A= XP_011516478.1:p.Ser1053=
XM_011518177.1:c.3153A= XP_011516479.1:p.Ser1051=
XM_011518178.1:c.2808A= XP_011516480.1:p.Ser936=
XM_011518179.1:c.2808A= XP_011516481.1:p.Ser936=
XM_011518180.1:c.2409A= XP_011516482.1:p.Ser803=
XM_011518176.3:c.3159A= XP_011516478.1:p.Ser1053=
XM_011518178.2:c.2808A= XP_011516480.1:p.Ser936=
XM_017014232.1:c.4131A= XP_016869721.1:p.Ser1377=
XM_017014233.1:c.3753A= XP_016869722.1:p.Ser1251=
XM_017014234.2:c.3153A= XP_016869723.1:p.Ser1051=
NM_139026.5:c.3882A= NP_620595.1:p.Ser1294=
NM_139027.5:c.3975A= NP_620596.2:p.Ser1325=
NM_139025.5:c.4143A= NP_620594.1:p.Ser1381=
NM_139026.6:c.3882A= NP_620595.1:p.Ser1294=
NM_139027.6:c.3975A= MANE Select NP_620596.2:p.Ser1325=
NR_024514.3:n.2627A=