Canonical Allele Identifier: CA2657954651
Gene: MYCN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945511_15945531dup , CM000664.2:g.15945511_15945531dup GRCh38
NC_000002.11:g.16085633_16085653dup , CM000664.1:g.16085633_16085653dup GRCh37
NC_000002.10:g.16003084_16003104dup NCBI36
NG_007457.1:g.9951_9971dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.158_178dup
ENST00000281043.4:c.809_829dup MANE Select ENSP00000281043.3:p.Glu276_Ile277insLysGluAspGluGluGluGlu
ENST00000638417.1:c.176_196dup ENSP00000491476.1:p.Glu65_Ile66insLysGluAspGluGluGluGlu
ENST00000281043.3:c.809_829dup ENSP00000281043.3:p.Glu276_Ile277insLysGluAspGluGluGluGlu
NM_001293228.1:c.809_829dup NP_001280157.1:p.Glu276_Ile277insLysGluAspGluGluGluGlu
NM_001293231.1:c.176_196dup NP_001280160.1:p.Glu65_Ile66insLysGluAspGluGluGluGlu
NM_001293233.1:c.*744_*764dup NP_001280162.1:n.*744_*764dup
NM_005378.5:c.809_829dup NP_005369.2:p.Glu276_Ile277insLysGluAspGluGluGluGlu
NM_005378.6:c.809_829dup MANE Select NP_005369.2:p.Glu276_Ile277insLysGluAspGluGluGluGlu
NM_001293228.2:c.809_829dup NP_001280157.1:p.Glu276_Ile277insLysGluAspGluGluGluGlu
NM_001293231.2:c.176_196dup NP_001280160.1:p.Glu65_Ile66insLysGluAspGluGluGluGlu
NM_001293233.2:c.*744_*764dup NP_001280162.1:n.*744_*764dup