Canonical Allele Identifier: CA1290852276
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856562_135856567delinsCTTTAT , CM000664.2:g.135856562_135856567delinsCTTTAT GRCh38
NC_000002.11:g.136614132_136614137delinsCTTTAT , CM000664.1:g.136614132_136614137delinsCTTTAT GRCh37
NC_000002.10:g.136330602_136330607delinsCTTTAT NCBI36
NG_008104.2:g.3603_3608delinsATAAAG , LRG_338:g.3603_3608delinsATAAAG
NG_008958.1:g.24875_24880delinsATAAAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1626+161_1626+166delinsATAAAG MANE Select ENSP00000264156.2:n.1626+161_1626+166delinsATAAAG
ENST00000264156.2:c.1626+161_1626+166delinsATAAAG ENSP00000264156.2:n.1626+161_1626+166delinsATAAAG
ENST00000492091.1:n.182-5004_182-4999delinsATAAAG
NM_005915.5:c.1626+161_1626+166delinsATAAAG NP_005906.2:n.1626+161_1626+166delinsATAAAG
NM_005915.6:c.1626+161_1626+166delinsATAAAG MANE Select NP_005906.2:n.1626+161_1626+166delinsATAAAG