Canonical Allele Identifier: CA2491131081

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945567T= , CM000664.2:g.15945567T=	GRCh38
NC_000002.11:g.16085689T= , CM000664.1:g.16085689T=	GRCh37
NC_000002.10:g.16003140T=	NCBI36
NG_007457.1:g.10007T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.214T=
ENST00000281043.4:c.865T= MANE Select	ENSP00000281043.3:p.Ser289=
ENST00000638417.1:c.232T=	ENSP00000491476.1:p.Ser78=
ENST00000281043.3:c.865T=	ENSP00000281043.3:p.Ser289=
NM_001293228.1:c.865T=	NP_001280157.1:p.Ser289=
NM_001293231.1:c.232T=	NP_001280160.1:p.Ser78=
NM_001293233.1:c.*800T=	NP_001280162.1:n.*800T=
NM_005378.5:c.865T=	NP_005369.2:p.Ser289=
NM_005378.6:c.865T= MANE Select	NP_005369.2:p.Ser289=
NM_001293228.2:c.865T=	NP_001280157.1:p.Ser289=
NM_001293231.2:c.232T=	NP_001280160.1:p.Ser78=
NM_001293233.2:c.*800T=	NP_001280162.1:n.*800T=