Canonical Allele Identifier: CA2491131122

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945650C= , CM000664.2:g.15945650C=	GRCh38
NC_000002.11:g.16085772C= , CM000664.1:g.16085772C=	GRCh37
NC_000002.10:g.16003223C=	NCBI36
NG_007457.1:g.10090C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.297C=
ENST00000281043.4:c.948C= MANE Select	ENSP00000281043.3:p.Ser316=
ENST00000638417.1:c.315C=	ENSP00000491476.1:p.Ser105=
ENST00000281043.3:c.948C=	ENSP00000281043.3:p.Ser316=
NM_001293228.1:c.948C=	NP_001280157.1:p.Ser316=
NM_001293231.1:c.315C=	NP_001280160.1:p.Ser105=
NM_001293233.1:c.*883C=	NP_001280162.1:n.*883C=
NM_005378.5:c.948C=	NP_005369.2:p.Ser316=
NM_005378.6:c.948C= MANE Select	NP_005369.2:p.Ser316=
NM_001293228.2:c.948C=	NP_001280157.1:p.Ser316=
NM_001293231.2:c.315C=	NP_001280160.1:p.Ser105=
NM_001293233.2:c.*883C=	NP_001280162.1:n.*883C=