Canonical Allele Identifier: CA2491131048

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945509_15945512delinsAGAG , CM000664.2:g.15945509_15945512delinsAGAG	GRCh38
NC_000002.11:g.16085631_16085634delinsAGAG , CM000664.1:g.16085631_16085634delinsAGAG	GRCh37
NC_000002.10:g.16003082_16003085delinsAGAG	NCBI36
NG_007457.1:g.9949_9952delinsAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.156_159delinsAGAG
ENST00000281043.4:c.807_810delinsAGAG MANE Select	ENSP00000281043.3:p.Glu269=
ENST00000638417.1:c.174_177delinsAGAG	ENSP00000491476.1:p.Glu58=
ENST00000281043.3:c.807_810delinsAGAG	ENSP00000281043.3:p.Glu269=
NM_001293228.1:c.807_810delinsAGAG	NP_001280157.1:p.Glu269=
NM_001293231.1:c.174_177delinsAGAG	NP_001280160.1:p.Glu58=
NM_001293233.1:c.*742_*745delinsAGAG	NP_001280162.1:n.*742_*745delinsAGAG
NM_005378.5:c.807_810delinsAGAG	NP_005369.2:p.Glu269=
NM_005378.6:c.807_810delinsAGAG MANE Select	NP_005369.2:p.Glu269=
NM_001293228.2:c.807_810delinsAGAG	NP_001280157.1:p.Glu269=
NM_001293231.2:c.174_177delinsAGAG	NP_001280160.1:p.Glu58=
NM_001293233.2:c.*742_*745delinsAGAG	NP_001280162.1:n.*742_*745delinsAGAG