Canonical Allele Identifier: CA2491131051

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945515A= , CM000664.2:g.15945515A=	GRCh38
NC_000002.11:g.16085637A= , CM000664.1:g.16085637A=	GRCh37
NC_000002.10:g.16003088A=	NCBI36
NG_007457.1:g.9955A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.162A=
ENST00000281043.4:c.813A= MANE Select	ENSP00000281043.3:p.Glu271=
ENST00000638417.1:c.180A=	ENSP00000491476.1:p.Glu60=
ENST00000281043.3:c.813A=	ENSP00000281043.3:p.Glu271=
NM_001293228.1:c.813A=	NP_001280157.1:p.Glu271=
NM_001293231.1:c.180A=	NP_001280160.1:p.Glu60=
NM_001293233.1:c.*748A=	NP_001280162.1:n.*748A=
NM_005378.5:c.813A=	NP_005369.2:p.Glu271=
NM_005378.6:c.813A= MANE Select	NP_005369.2:p.Glu271=
NM_001293228.2:c.813A=	NP_001280157.1:p.Glu271=
NM_001293231.2:c.180A=	NP_001280160.1:p.Glu60=
NM_001293233.2:c.*748A=	NP_001280162.1:n.*748A=