Canonical Allele Identifier: CA2657954650
Gene: MYCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945509_15945511del , CM000664.2:g.15945509_15945511del GRCh38
NC_000002.11:g.16085631_16085633del , CM000664.1:g.16085631_16085633del GRCh37
NC_000002.10:g.16003082_16003084del NCBI36
NG_007457.1:g.9949_9951del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.156_158del
ENST00000281043.4:c.807_809del MANE Select ENSP00000281043.3:p.Glu270del
ENST00000638417.1:c.174_176del ENSP00000491476.1:p.Glu59del
ENST00000281043.3:c.807_809del ENSP00000281043.3:p.Glu270del
NM_001293228.1:c.807_809del NP_001280157.1:p.Glu270del
NM_001293231.1:c.174_176del NP_001280160.1:p.Glu59del
NM_001293233.1:c.*742_*744del NP_001280162.1:n.*742_*744del
NM_005378.5:c.807_809del NP_005369.2:p.Glu270del
NM_005378.6:c.807_809del MANE Select NP_005369.2:p.Glu270del
NM_001293228.2:c.807_809del NP_001280157.1:p.Glu270del
NM_001293231.2:c.174_176del NP_001280160.1:p.Glu59del
NM_001293233.2:c.*742_*744del NP_001280162.1:n.*742_*744del