Canonical Allele Identifier: CA10588312
Gene: MYCN HGNC NCBI

Linked Data

ClinVar Variation Id: 265250
ClinVar RCV Id: RCV000255968
dbSNP Id: rs886039427

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15942575_15942615del , CM000664.2:g.15942575_15942615del GRCh38
NC_000002.11:g.16082697_16082737del , CM000664.1:g.16082697_16082737del GRCh37
NC_000002.10:g.16000148_16000188del NCBI36
NG_007457.1:g.7015_7055del

Transcript Alleles

HGVS Amino-acid change
ENST00000281043.4:c.511_551del MANE Select ENSP00000281043.3:p.Ala171ArgfsTer?
ENST00000638417.1:c.157+1832_157+1872del ENSP00000491476.1:n.157+1832_157+1872del
ENST00000281043.3:c.511_551del ENSP00000281043.3:p.Ala171ArgfsTer?
NM_001293228.1:c.511_551del NP_001280157.1:p.Ala171ArgfsTer?
NM_001293231.1:c.157+1832_157+1872del NP_001280160.1:n.157+1832_157+1872del
NM_001293233.1:c.*446_*486del NP_001280162.1:n.*446_*486del
NM_005378.5:c.511_551del NP_005369.2:p.Ala171ArgfsTer?
NM_005378.6:c.511_551del MANE Select NP_005369.2:p.Ala171ArgfsTer?
NM_001293228.2:c.511_551del NP_001280157.1:p.Ala171ArgfsTer?
NM_001293231.2:c.157+1832_157+1872del NP_001280160.1:n.157+1832_157+1872del
NM_001293233.2:c.*446_*486del NP_001280162.1:n.*446_*486del