Canonical Allele Identifier: CA1781909311
Gene: MCM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960399_47960401delinsCAA , CM000670.2:g.47960399_47960401delinsCAA GRCh38
NC_000008.10:g.48872959_48872961delinsCAA , CM000670.1:g.48872959_48872961delinsCAA GRCh37
NC_000008.9:g.49035512_49035514delinsCAA NCBI36
NG_023435.1:g.4783_4785delinsTTG , LRG_162:g.4783_4785delinsTTG
NG_032967.1:g.5197_5199delinsCAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+79_-15+81delinsCAA ENSP00000430329.1:n.-15+79_-15+81delinsCAA
NM_005914.3:c.-746_-744delinsCAA NP_005905.2:n.-746_-744delinsCAA
NM_182746.2:c.-630_-628delinsCAA NP_877423.1:n.-630_-628delinsCAA
XM_005251234.1:c.-992_-990delinsCAA XP_005251291.1:n.-992_-990delinsCAA