Canonical Allele Identifier: CA2491131059

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945525G= , CM000664.2:g.15945525G=	GRCh38
NC_000002.11:g.16085647G= , CM000664.1:g.16085647G=	GRCh37
NC_000002.10:g.16003098G=	NCBI36
NG_007457.1:g.9965G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.172G=
ENST00000281043.4:c.823G= MANE Select	ENSP00000281043.3:p.Glu275=
ENST00000638417.1:c.190G=	ENSP00000491476.1:p.Glu64=
ENST00000281043.3:c.823G=	ENSP00000281043.3:p.Glu275=
NM_001293228.1:c.823G=	NP_001280157.1:p.Glu275=
NM_001293231.1:c.190G=	NP_001280160.1:p.Glu64=
NM_001293233.1:c.*758G=	NP_001280162.1:n.*758G=
NM_005378.5:c.823G=	NP_005369.2:p.Glu275=
NM_005378.6:c.823G= MANE Select	NP_005369.2:p.Glu275=
NM_001293228.2:c.823G=	NP_001280157.1:p.Glu275=
NM_001293231.2:c.190G=	NP_001280160.1:p.Glu64=
NM_001293233.2:c.*758G=	NP_001280162.1:n.*758G=