Canonical Allele Identifier: CA1781909367
Gene: MCM4 HGNC NCBI

Linked Data

dbSNP Id: rs2090798855

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.47960475_47960476insTGCA , CM000670.2:g.47960475_47960476insTGCA GRCh38
NC_000008.10:g.48873035_48873036insTGCA , CM000670.1:g.48873035_48873036insTGCA GRCh37
NC_000008.9:g.49035588_49035589insTGCA NCBI36
NG_023435.1:g.4708_4709insTGCA , LRG_162:g.4708_4709insTGCA
NG_032967.1:g.5273_5274insTGCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000518221.5:c.-15+155_-15+156insTGCA ENSP00000430329.1:n.-15+155_-15+156insTGCA
NM_005914.3:c.-670_-669insTGCA NP_005905.2:n.-670_-669insTGCA
NM_182746.2:c.-554_-553insTGCA NP_877423.1:n.-554_-553insTGCA
XM_005251234.1:c.-916_-915insTGCA XP_005251291.1:n.-916_-915insTGCA