Canonical Allele Identifier: CA10602809

Gene: MYCN

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.15942506del , CM000664.2:g.15942506del	GRCh38
NC_000002.11:g.16082628del , CM000664.1:g.16082628del	GRCh37
NC_000002.10:g.16000079del	NCBI36
NG_007457.1:g.6946del

Transcript Alleles

HGVS	Amino-acid Change
NM_005378.6:c.442del MANE Select	NP_005369.2:p.Gln148SerfsTer?
ENST00000281043.4:c.442del MANE Select	ENSP00000281043.3:p.Gln148SerfsTer?
NM_001293228.1:c.442del	NP_001280157.1:p.Gln148SerfsTer?
NM_001293228.2:c.442del	NP_001280157.1:p.Gln148SerfsTer?
NM_001293231.1:c.157+1763del	NP_001280160.1:n.157+1763del
NM_001293231.2:c.157+1763del	NP_001280160.1:n.157+1763del
NM_001293233.1:c.*377del	NP_001280162.1:n.*377del
NM_001293233.2:c.*377del	NP_001280162.1:n.*377del
NM_005378.5:c.442del	NP_005369.2:p.Gln148SerfsTer?
ENST00000281043.3:c.442del	ENSP00000281043.3:p.Gln148SerfsTer?
ENST00000638417.1:c.157+1763del	ENSP00000491476.1:n.157+1763del