Canonical Allele Identifier: CA1365145667
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.53057101_53057103delinsTCC , CM000665.2:g.53057101_53057103delinsTCC GRCh38
NC_000003.11:g.53091117_53091119delinsTCC , CM000665.1:g.53091117_53091119delinsTCC GRCh37
NC_000003.10:g.53066157_53066159delinsTCC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000607203.1:c.318-9864_318-9862delinsGGA
ENST00000607283.5:c.465-13849_465-13847delinsGGA
ENST00000607495.5:c.447+20585_447+20587delinsGGA