Canonical Allele Identifier: CA2586968722

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945799dup , CM000664.2:g.15945799dup	GRCh38
NC_000002.11:g.16085921dup , CM000664.1:g.16085921dup	GRCh37
NC_000002.10:g.16003372dup	NCBI36
NG_007457.1:g.10239dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.446dup
ENST00000281043.4:c.1097dup MANE Select	ENSP00000281043.3:p.Ala367GlyfsTer2
ENST00000638417.1:c.464dup	ENSP00000491476.1:p.Ala156GlyfsTer2
ENST00000281043.3:c.1097dup	ENSP00000281043.3:p.Ala367GlyfsTer2
NM_001293228.1:c.1097dup	NP_001280157.1:p.Ala367GlyfsTer2
NM_001293231.1:c.464dup	NP_001280160.1:p.Ala156GlyfsTer2
NM_001293233.1:c.*1032dup	NP_001280162.1:n.*1032dup
NM_005378.5:c.1097dup	NP_005369.2:p.Ala367GlyfsTer2
NM_005378.6:c.1097dup MANE Select	NP_005369.2:p.Ala367GlyfsTer2
NM_001293228.2:c.1097dup	NP_001280157.1:p.Ala367GlyfsTer2
NM_001293231.2:c.464dup	NP_001280160.1:p.Ala156GlyfsTer2
NM_001293233.2:c.*1032dup	NP_001280162.1:n.*1032dup