Canonical Allele Identifier: CA2576682128

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945829_15945830insGT , CM000664.2:g.15945829_15945830insGT	GRCh38
NC_000002.11:g.16085951_16085952insGT , CM000664.1:g.16085951_16085952insGT	GRCh37
NC_000002.10:g.16003402_16003403insGT	NCBI36
NG_007457.1:g.10269_10270insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.476_477insGT
ENST00000281043.4:c.1127_1128insGT MANE Select	ENSP00000281043.3:p.Asp376GlufsTer?
ENST00000638417.1:c.494_495insGT	ENSP00000491476.1:p.Asp165GlufsTer?
ENST00000281043.3:c.1127_1128insGT	ENSP00000281043.3:p.Asp376GlufsTer?
NM_001293228.1:c.1127_1128insGT	NP_001280157.1:p.Asp376GlufsTer?
NM_001293231.1:c.494_495insGT	NP_001280160.1:p.Asp165GlufsTer?
NM_001293233.1:c.*1062_*1063insGT	NP_001280162.1:n.*1062_*1063insGT
NM_005378.5:c.1127_1128insGT	NP_005369.2:p.Asp376GlufsTer?
NM_005378.6:c.1127_1128insGT MANE Select	NP_005369.2:p.Asp376GlufsTer?
NM_001293228.2:c.1127_1128insGT	NP_001280157.1:p.Asp376GlufsTer?
NM_001293231.2:c.494_495insGT	NP_001280160.1:p.Asp165GlufsTer?
NM_001293233.2:c.*1062_*1063insGT	NP_001280162.1:n.*1062_*1063insGT