Canonical Allele Identifier: CA2491131061

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945533C= , CM000664.2:g.15945533C=	GRCh38
NC_000002.11:g.16085655C= , CM000664.1:g.16085655C=	GRCh37
NC_000002.10:g.16003106C=	NCBI36
NG_007457.1:g.9973C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.180C=
ENST00000281043.4:c.831C= MANE Select	ENSP00000281043.3:p.Ile277=
ENST00000638417.1:c.198C=	ENSP00000491476.1:p.Ile66=
ENST00000281043.3:c.831C=	ENSP00000281043.3:p.Ile277=
NM_001293228.1:c.831C=	NP_001280157.1:p.Ile277=
NM_001293231.1:c.198C=	NP_001280160.1:p.Ile66=
NM_001293233.1:c.*766C=	NP_001280162.1:n.*766C=
NM_005378.5:c.831C=	NP_005369.2:p.Ile277=
NM_005378.6:c.831C= MANE Select	NP_005369.2:p.Ile277=
NM_001293228.2:c.831C=	NP_001280157.1:p.Ile277=
NM_001293231.2:c.198C=	NP_001280160.1:p.Ile66=
NM_001293233.2:c.*766C=	NP_001280162.1:n.*766C=