Canonical Allele Identifier: CA918256054
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs1589824615

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960472_47960473insGCCTGC , CM000670.2:g.47960472_47960473insGCCTGC GRCh38
NC_000008.10:g.48873032_48873033insGCCTGC , CM000670.1:g.48873032_48873033insGCCTGC GRCh37
NC_000008.9:g.49035585_49035586insGCCTGC NCBI36
NG_023435.1:g.4712_4713insCAGGCG , LRG_162:g.4712_4713insCAGGCG
NG_032967.1:g.5270_5271insGCCTGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+152_-15+153insGCCTGC ENSP00000430329.1:n.-15+152_-15+153insGCCTGC
NM_005914.3:c.-673_-672insGCCTGC NP_005905.2:n.-673_-672insGCCTGC
NM_182746.2:c.-557_-556insGCCTGC NP_877423.1:n.-557_-556insGCCTGC
XM_005251234.1:c.-919_-918insGCCTGC XP_005251291.1:n.-919_-918insGCCTGC