Canonical Allele Identifier: CA2491131070

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15945547_15945550delinsTGGA , CM000664.2:g.15945547_15945550delinsTGGA	GRCh38
NC_000002.11:g.16085669_16085672delinsTGGA , CM000664.1:g.16085669_16085672delinsTGGA	GRCh37
NC_000002.10:g.16003120_16003123delinsTGGA	NCBI36
NG_007457.1:g.9987_9990delinsTGGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000703162.1:n.194_197delinsTGGA
ENST00000281043.4:c.845_848delinsTGGA MANE Select	ENSP00000281043.3:p.Val282=
ENST00000638417.1:c.212_215delinsTGGA	ENSP00000491476.1:p.Val71=
ENST00000281043.3:c.845_848delinsTGGA	ENSP00000281043.3:p.Val282=
NM_001293228.1:c.845_848delinsTGGA	NP_001280157.1:p.Val282=
NM_001293231.1:c.212_215delinsTGGA	NP_001280160.1:p.Val71=
NM_001293233.1:c.*780_*783delinsTGGA	NP_001280162.1:n.*780_*783delinsTGGA
NM_005378.5:c.845_848delinsTGGA	NP_005369.2:p.Val282=
NM_005378.6:c.845_848delinsTGGA MANE Select	NP_005369.2:p.Val282=
NM_001293228.2:c.845_848delinsTGGA	NP_001280157.1:p.Val282=
NM_001293231.2:c.212_215delinsTGGA	NP_001280160.1:p.Val71=
NM_001293233.2:c.*780_*783delinsTGGA	NP_001280162.1:n.*780_*783delinsTGGA