Canonical Allele Identifier: CA2491131086

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945578G= , CM000664.2:g.15945578G=	GRCh38
NC_000002.11:g.16085700G= , CM000664.1:g.16085700G=	GRCh37
NC_000002.10:g.16003151G=	NCBI36
NG_007457.1:g.10018G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.225G=
ENST00000281043.4:c.876G= MANE Select	ENSP00000281043.3:p.Lys292=
ENST00000638417.1:c.243G=	ENSP00000491476.1:p.Lys81=
ENST00000281043.3:c.876G=	ENSP00000281043.3:p.Lys292=
NM_001293228.1:c.876G=	NP_001280157.1:p.Lys292=
NM_001293231.1:c.243G=	NP_001280160.1:p.Lys81=
NM_001293233.1:c.*811G=	NP_001280162.1:n.*811G=
NM_005378.5:c.876G=	NP_005369.2:p.Lys292=
NM_005378.6:c.876G= MANE Select	NP_005369.2:p.Lys292=
NM_001293228.2:c.876G=	NP_001280157.1:p.Lys292=
NM_001293231.2:c.243G=	NP_001280160.1:p.Lys81=
NM_001293233.2:c.*811G=	NP_001280162.1:n.*811G=