Canonical Allele Identifier: CA2695200426
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2637010
ClinVar RCV Id: RCV003394370
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945603del , CM000664.2:g.15945603del GRCh38
NC_000002.11:g.16085725del , CM000664.1:g.16085725del GRCh37
NC_000002.10:g.16003176del NCBI36
NG_007457.1:g.10043del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.250del
ENST00000281043.4:c.901del MANE Select ENSP00000281043.3:p.Val301CysfsTer18
ENST00000638417.1:c.268del ENSP00000491476.1:p.Val90CysfsTer18
ENST00000281043.3:c.901del ENSP00000281043.3:p.Val301CysfsTer18
NM_001293228.1:c.901del NP_001280157.1:p.Val301CysfsTer18
NM_001293231.1:c.268del NP_001280160.1:p.Val90CysfsTer18
NM_001293233.1:c.*836del NP_001280162.1:n.*836del
NM_005378.5:c.901del NP_005369.2:p.Val301CysfsTer18
NM_005378.6:c.901del MANE Select NP_005369.2:p.Val301CysfsTer18
NM_001293228.2:c.901del NP_001280157.1:p.Val301CysfsTer18
NM_001293231.2:c.268del NP_001280160.1:p.Val90CysfsTer18
NM_001293233.2:c.*836del NP_001280162.1:n.*836del
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