Canonical Allele Identifier: CA375707266
Gene: ADAMTS13 HGNC NCBI
gnomAD v4:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133424452C>A , CM000671.2:g.133424452C>A GRCh38
NC_000009.10:g.135279393C>A NCBI36
NG_011934.2:g.15114C>A , LRG_544:g.15114C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355699.7:c.304C>A MANE Select ENSP00000347927.2:p.Arg102Ser
ENST00000355699.6:c.304C>A ENSP00000347927.2:p.Arg102Ser
ENST00000356589.6:c.304C>A ENSP00000348997.2:p.Arg102Ser
ENST00000371911.7:c.304C>A ENSP00000360979.3:p.Arg102Ser
ENST00000371916.5:c.-441C>A ENSP00000360984.2:n.-441C>A
ENST00000371929.7:c.304C>A ENSP00000360997.3:p.Arg102Ser
ENST00000474918.1:c.304C>A ENSP00000435305.1:p.Arg102Ser
ENST00000485925.5:n.486C>A
ENST00000495234.5:c.304C>A ENSP00000435274.1:p.Arg102Ser
NM_139025.4:c.304C>A , LRG_544t1:c.304C>A NP_620594.1:p.Arg102Ser
NM_139026.4:c.304C>A NP_620595.1:p.Arg102Ser
NM_139027.4:c.304C>A NP_620596.2:p.Arg102Ser
NR_024514.2:n.505C>A
XM_011518174.1:c.-87C>A XP_011516476.1:n.-87C>A
XM_011518175.1:c.304C>A XP_011516477.1:p.Arg102Ser
XM_011518180.1:c.304C>A XP_011516482.1:p.Arg102Ser
XM_017014232.1:c.292C>A XP_016869721.1:p.Arg98Ser
XM_017014233.1:c.-87C>A XP_016869722.1:n.-87C>A
XM_017014235.1:c.304C>A XP_016869724.1:p.Arg102Ser
XR_001746171.1:n.1529C>A
NM_139026.5:c.304C>A NP_620595.1:p.Arg102Ser
NM_139027.5:c.304C>A NP_620596.2:p.Arg102Ser
NM_139025.5:c.304C>A NP_620594.1:p.Arg102Ser
NM_139026.6:c.304C>A NP_620595.1:p.Arg102Ser
NM_139027.6:c.304C>A MANE Select NP_620596.2:p.Arg102Ser
NR_024514.3:n.507C>A