Canonical Allele Identifier: CA1290849614
Gene: MCM6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.135850899_135850900delinsAG , CM000664.2:g.135850899_135850900delinsAG GRCh38
NC_000002.11:g.136608469_136608470delinsAG , CM000664.1:g.136608469_136608470delinsAG GRCh37
NC_000002.10:g.136324939_136324940delinsAG NCBI36
NG_008104.2:g.9270_9271delinsCT , LRG_338:g.9270_9271delinsCT
NG_008958.1:g.30542_30543delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000264156.3:c.1917+502_1917+503delinsCT MANE Select ENSP00000264156.2:n.1917+502_1917+503delinsCT
ENST00000264156.2:c.1917+502_1917+503delinsCT ENSP00000264156.2:n.1917+502_1917+503delinsCT
ENST00000483902.1:n.544+502_544+503delinsCT
ENST00000492091.1:n.343+502_343+503delinsCT
NM_005915.5:c.1917+502_1917+503delinsCT NP_005906.2:n.1917+502_1917+503delinsCT
NM_005915.6:c.1917+502_1917+503delinsCT MANE Select NP_005906.2:n.1917+502_1917+503delinsCT