Canonical Allele Identifier: CA1290852259
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856540_135856541delinsGT , CM000664.2:g.135856540_135856541delinsGT GRCh38
NC_000002.11:g.136614110_136614111delinsGT , CM000664.1:g.136614110_136614111delinsGT GRCh37
NC_000002.10:g.136330580_136330581delinsGT NCBI36
NG_008104.2:g.3629_3630delinsAC , LRG_338:g.3629_3630delinsAC
NG_008958.1:g.24901_24902delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+187_1626+188delinsAC MANE Select ENSP00000264156.2:n.1626+187_1626+188delinsAC
ENST00000264156.2:c.1626+187_1626+188delinsAC ENSP00000264156.2:n.1626+187_1626+188delinsAC
ENST00000492091.1:n.182-4978_182-4977delinsAC
NM_005915.5:c.1626+187_1626+188delinsAC NP_005906.2:n.1626+187_1626+188delinsAC
NM_005915.6:c.1626+187_1626+188delinsAC MANE Select NP_005906.2:n.1626+187_1626+188delinsAC