Canonical Allele Identifier: CA2491131117

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945632C= , CM000664.2:g.15945632C=	GRCh38
NC_000002.11:g.16085754C= , CM000664.1:g.16085754C=	GRCh37
NC_000002.10:g.16003205C=	NCBI36
NG_007457.1:g.10072C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.279C=
ENST00000281043.4:c.930C= MANE Select	ENSP00000281043.3:p.Pro310=
ENST00000638417.1:c.297C=	ENSP00000491476.1:p.Pro99=
ENST00000281043.3:c.930C=	ENSP00000281043.3:p.Pro310=
NM_001293228.1:c.930C=	NP_001280157.1:p.Pro310=
NM_001293231.1:c.297C=	NP_001280160.1:p.Pro99=
NM_001293233.1:c.*865C=	NP_001280162.1:n.*865C=
NM_005378.5:c.930C=	NP_005369.2:p.Pro310=
NM_005378.6:c.930C= MANE Select	NP_005369.2:p.Pro310=
NM_001293228.2:c.930C=	NP_001280157.1:p.Pro310=
NM_001293231.2:c.297C=	NP_001280160.1:p.Pro99=
NM_001293233.2:c.*865C=	NP_001280162.1:n.*865C=