Canonical Allele Identifier: CA2661278952
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856685_135856686insGAGT , CM000664.2:g.135856685_135856686insGAGT GRCh38
NC_000002.11:g.136614255_136614256insGAGT , CM000664.1:g.136614255_136614256insGAGT GRCh37
NC_000002.10:g.136330725_136330726insGAGT NCBI36
NG_008104.2:g.3484_3485insACTC , LRG_338:g.3484_3485insACTC
NG_008958.1:g.24756_24757insACTC

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+42_1626+43insACTC MANE Select ENSP00000264156.2:n.1626+42_1626+43insACT...
ENST00000264156.2:c.1626+42_1626+43insACTC ENSP00000264156.2:n.1626+42_1626+43insACT...
ENST00000492091.1:n.182-5123_182-5122insACTC
NM_005915.5:c.1626+42_1626+43insACTC NP_005906.2:n.1626+42_1626+43insACTC
NM_005915.6:c.1626+42_1626+43insACTC MANE Select NP_005906.2:n.1626+42_1626+43insACTC