Canonical Allele Identifier: CA2491131052

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945518T= , CM000664.2:g.15945518T=	GRCh38
NC_000002.11:g.16085640T= , CM000664.1:g.16085640T=	GRCh37
NC_000002.10:g.16003091T=	NCBI36
NG_007457.1:g.9958T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.165T=
ENST00000281043.4:c.816T= MANE Select	ENSP00000281043.3:p.Asp272=
ENST00000638417.1:c.183T=	ENSP00000491476.1:p.Asp61=
ENST00000281043.3:c.816T=	ENSP00000281043.3:p.Asp272=
NM_001293228.1:c.816T=	NP_001280157.1:p.Asp272=
NM_001293231.1:c.183T=	NP_001280160.1:p.Asp61=
NM_001293233.1:c.*751T=	NP_001280162.1:n.*751T=
NM_005378.5:c.816T=	NP_005369.2:p.Asp272=
NM_005378.6:c.816T= MANE Select	NP_005369.2:p.Asp272=
NM_001293228.2:c.816T=	NP_001280157.1:p.Asp272=
NM_001293231.2:c.183T=	NP_001280160.1:p.Asp61=
NM_001293233.2:c.*751T=	NP_001280162.1:n.*751T=