Canonical Allele Identifier: CA1290852243
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856500_135856501delinsAG , CM000664.2:g.135856500_135856501delinsAG GRCh38
NC_000002.11:g.136614070_136614071delinsAG , CM000664.1:g.136614070_136614071delinsAG GRCh37
NC_000002.10:g.136330540_136330541delinsAG NCBI36
NG_008104.2:g.3669_3670delinsCT , LRG_338:g.3669_3670delinsCT
NG_008958.1:g.24941_24942delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1626+227_1626+228delinsCT MANE Select ENSP00000264156.2:n.1626+227_1626+228delinsCT
ENST00000264156.2:c.1626+227_1626+228delinsCT ENSP00000264156.2:n.1626+227_1626+228delinsCT
ENST00000492091.1:n.182-4938_182-4937delinsCT
NM_005915.5:c.1626+227_1626+228delinsCT NP_005906.2:n.1626+227_1626+228delinsCT
NM_005915.6:c.1626+227_1626+228delinsCT MANE Select NP_005906.2:n.1626+227_1626+228delinsCT