Canonical Allele Identifier: CA2661278858
Gene: MCM6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135856645_135856646insGGGCTGGTGCACATACATGCAC , CM000664.2:g.135856645_135856646insGGGCTGGTGCACATACATGCAC GRCh38
NC_000002.11:g.136614215_136614216insGGGCTGGTGCACATACATGCAC , CM000664.1:g.136614215_136614216insGGGCTGGTGCACATACATGCAC GRCh37
NC_000002.10:g.136330685_136330686insGGGCTGGTGCACATACATGCAC NCBI36
NG_008104.2:g.3545_3546insCGTGCATGTATGTGCACCAGCC , LRG_338:g.3545_3546insCGTGCATGTATGTGCACCAGCC
NG_008958.1:g.24817_24818insCGTGCATGTATGTGCACCAGCC

Transcript Alleles

HGVS Amino-acid change
ENST00000264156.3:c.1626+103_1626+104insCGTGCATGTATGTGCACCAGCC MANE Select ENSP00000264156.2:n.1626+103_1626+104insCGTGCATGTATGTGCACCAGC...
ENST00000264156.2:c.1626+103_1626+104insCGTGCATGTATGTGCACCAGCC ENSP00000264156.2:n.1626+103_1626+104insCGTGCATGTATGTGCACCAGC...
ENST00000492091.1:n.182-5062_182-5061insCGTGCATGTATGTGCACCAGCC
NM_005915.5:c.1626+103_1626+104insCGTGCATGTATGTGCACCAGCC NP_005906.2:n.1626+103_1626+104insCGTGCATGTATGTGCACCAGCC
NM_005915.6:c.1626+103_1626+104insCGTGCATGTATGTGCACCAGCC MANE Select NP_005906.2:n.1626+103_1626+104insCGTGCATGTATGTGCACCAGCC