Canonical Allele Identifier: CA1036810352

Gene: MCM6

Linked Data

• gnomAD v3: 2-135850896-C-CGGGGGGGGGGGGGGGGGGG
• gnomAD v4: 2-135850896-C-CGGGGGGGGGGGGGGGGGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.135850897_135850898insGGGGGGGGGGGGGGGGGGG , CM000664.2:g.135850897_135850898insGGGGGGGGGGGGGGGGGGG	GRCh38
NC_000002.11:g.136608467_136608468insGGGGGGGGGGGGGGGGGGG , CM000664.1:g.136608467_136608468insGGGGGGGGGGGGGGGGGGG	GRCh37
NC_000002.10:g.136324937_136324938insGGGGGGGGGGGGGGGGGGG	NCBI36
NG_008104.2:g.9273_9274insCCCCCCCCCCCCCCCCCCC , LRG_338:g.9273_9274insCCCCCCCCCCCCCCCCCCC
NG_008958.1:g.30545_30546insCCCCCCCCCCCCCCCCCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000264156.3:c.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC MANE Select	ENSP00000264156.2:n.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC
ENST00000264156.2:c.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC	ENSP00000264156.2:n.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC
ENST00000483902.1:n.544+505_544+506insCCCCCCCCCCCCCCCCCCC
ENST00000492091.1:n.343+505_343+506insCCCCCCCCCCCCCCCCCCC
NM_005915.5:c.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC	NP_005906.2:n.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC
NM_005915.6:c.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC MANE Select	NP_005906.2:n.1917+505_1917+506insCCCCCCCCCCCCCCCCCCC