Canonical Allele Identifier: CA2491131056

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945521A= , CM000664.2:g.15945521A=	GRCh38
NC_000002.11:g.16085643A= , CM000664.1:g.16085643A=	GRCh37
NC_000002.10:g.16003094A=	NCBI36
NG_007457.1:g.9961A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.168A=
ENST00000281043.4:c.819A= MANE Select	ENSP00000281043.3:p.Glu273=
ENST00000638417.1:c.186A=	ENSP00000491476.1:p.Glu62=
ENST00000281043.3:c.819A=	ENSP00000281043.3:p.Glu273=
NM_001293228.1:c.819A=	NP_001280157.1:p.Glu273=
NM_001293231.1:c.186A=	NP_001280160.1:p.Glu62=
NM_001293233.1:c.*754A=	NP_001280162.1:n.*754A=
NM_005378.5:c.819A=	NP_005369.2:p.Glu273=
NM_005378.6:c.819A= MANE Select	NP_005369.2:p.Glu273=
NM_001293228.2:c.819A=	NP_001280157.1:p.Glu273=
NM_001293231.2:c.186A=	NP_001280160.1:p.Glu62=
NM_001293233.2:c.*754A=	NP_001280162.1:n.*754A=