Canonical Allele Identifier: CA2491131114

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945625T= , CM000664.2:g.15945625T=	GRCh38
NC_000002.11:g.16085747T= , CM000664.1:g.16085747T=	GRCh37
NC_000002.10:g.16003198T=	NCBI36
NG_007457.1:g.10065T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.272T=
ENST00000281043.4:c.923T= MANE Select	ENSP00000281043.3:p.Leu308=
ENST00000638417.1:c.290T=	ENSP00000491476.1:p.Leu97=
ENST00000281043.3:c.923T=	ENSP00000281043.3:p.Leu308=
NM_001293228.1:c.923T=	NP_001280157.1:p.Leu308=
NM_001293231.1:c.290T=	NP_001280160.1:p.Leu97=
NM_001293233.1:c.*858T=	NP_001280162.1:n.*858T=
NM_005378.5:c.923T=	NP_005369.2:p.Leu308=
NM_005378.6:c.923T= MANE Select	NP_005369.2:p.Leu308=
NM_001293228.2:c.923T=	NP_001280157.1:p.Leu308=
NM_001293231.2:c.290T=	NP_001280160.1:p.Leu97=
NM_001293233.2:c.*858T=	NP_001280162.1:n.*858T=