Canonical Allele Identifier: CA276811415
Community Standard Title: NM_001761.3(CCNF):c.1094+105_1094+106dup
Gene: CCNF HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2445727_2445728dup , CM000678.2:g.2445727_2445728dup GRCh38
NC_000016.9:g.2495728_2495729dup , CM000678.1:g.2495728_2495729dup GRCh37
NC_000016.8:g.2435729_2435730dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_001761.3:c.1094+105_1094+106dup MANE Select NP_001752.2:n.1094+105_1094+106dup
ENST00000397066.9:c.1094+105_1094+106dup MANE Select ENSP00000380256.4:n.1094+105_1094+106dup
NM_001323538.1:c.170+105_170+106dup NP_001310467.1:n.170+105_170+106dup
NM_001323538.2:c.170+105_170+106dup NP_001310467.1:n.170+105_170+106dup
NM_001761.2:c.1094+105_1094+106dup NP_001752.2:n.1094+105_1094+106dup
ENST00000293968.11:c.*807+105_*807+106dup ENSP00000293968.7:n.*807+105_*807+106dup
ENST00000397066.8:c.1094+105_1094+106dup ENSP00000380256.4:n.1094+105_1094+106dup
ENST00000564236.1:c.265+105_265+106dup
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