Canonical Allele Identifier: CA2002397736
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.116072516_116072519delinsTTGC , CM000673.2:g.116072516_116072519delinsTTGC GRCh38
NC_000011.9:g.115943234_115943237delinsTTGC , CM000673.1:g.115943234_115943237delinsTTGC GRCh37
NC_000011.8:g.115448444_115448447delinsTTGC NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_948055.1:n.192+495_192+498delinsGCAA
XR_948056.1:n.311-5314_311-5311delinsGCAA
XR_948057.1:n.97+590_97+593delinsGCAA
XR_001748401.1:n.192+495_192+498delinsGCAA
XR_948055.2:n.192+495_192+498delinsGCAA
XR_948056.2:n.314-5314_314-5311delinsGCAA
XR_948057.2:n.97+590_97+593delinsGCAA