Canonical Allele Identifier: CA2586968718
Gene: MYCN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945617_15945618insT , CM000664.2:g.15945617_15945618insT GRCh38
NC_000002.11:g.16085739_16085740insT , CM000664.1:g.16085739_16085740insT GRCh37
NC_000002.10:g.16003190_16003191insT NCBI36
NG_007457.1:g.10057_10058insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.264_265insT
ENST00000281043.4:c.915_916insT MANE Select ENSP00000281043.3:p.Ala306CysfsTer?
ENST00000638417.1:c.282_283insT ENSP00000491476.1:p.Ala95CysfsTer?
ENST00000281043.3:c.915_916insT ENSP00000281043.3:p.Ala306CysfsTer?
NM_001293228.1:c.915_916insT NP_001280157.1:p.Ala306CysfsTer?
NM_001293231.1:c.282_283insT NP_001280160.1:p.Ala95CysfsTer?
NM_001293233.1:c.*850_*851insT NP_001280162.1:n.*850_*851insT
NM_005378.5:c.915_916insT NP_005369.2:p.Ala306CysfsTer?
NM_005378.6:c.915_916insT MANE Select NP_005369.2:p.Ala306CysfsTer?
NM_001293228.2:c.915_916insT NP_001280157.1:p.Ala306CysfsTer?
NM_001293231.2:c.282_283insT NP_001280160.1:p.Ala95CysfsTer?
NM_001293233.2:c.*850_*851insT NP_001280162.1:n.*850_*851insT