Canonical Allele Identifier: CA1365145670
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057107_53057108delinsCT , CM000665.2:g.53057107_53057108delinsCT GRCh38
NC_000003.11:g.53091123_53091124delinsCT , CM000665.1:g.53091123_53091124delinsCT GRCh37
NC_000003.10:g.53066163_53066164delinsCT NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9869_318-9868delinsAG
ENST00000607283.5:c.465-13854_465-13853delinsAG
ENST00000607495.5:c.447+20580_447+20581delinsAG