Canonical Allele Identifier: CA1290853424
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135859148_135859149delinsCT , CM000664.2:g.135859148_135859149delinsCT GRCh38
NC_000002.11:g.136616718_136616719delinsCT , CM000664.1:g.136616718_136616719delinsCT GRCh37
NC_000002.10:g.136333188_136333189delinsCT NCBI36
NG_008104.2:g.1021_1022delinsAG , LRG_338:g.1021_1022delinsAG
NG_008958.1:g.22293_22294delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1362+152_1362+153delinsAG MANE Select ENSP00000264156.2:n.1362+152_1362+153delinsAG
ENST00000264156.2:c.1362+152_1362+153delinsAG ENSP00000264156.2:n.1362+152_1362+153delinsAG
ENST00000492091.1:n.181+3458_181+3459delinsAG
NM_005915.5:c.1362+152_1362+153delinsAG NP_005906.2:n.1362+152_1362+153delinsAG
NM_005915.6:c.1362+152_1362+153delinsAG MANE Select NP_005906.2:n.1362+152_1362+153delinsAG