Canonical Allele Identifier: CA1538258
Gene: MYCN HGNC NCBI

Linked Data

dbSNP Id: rs768951879

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15945549_15945551del , CM000664.2:g.15945549_15945551del GRCh38
NC_000002.11:g.16085671_16085673del , CM000664.1:g.16085671_16085673del GRCh37
NC_000002.10:g.16003122_16003124del NCBI36
NG_007457.1:g.9989_9991del

Transcript Alleles

HGVS Amino-acid Change
ENST00000703162.1:n.196_198del
ENST00000281043.4:c.847_849del MANE Select ENSP00000281043.3:p.Glu283del
ENST00000638417.1:c.214_216del ENSP00000491476.1:p.Glu72del
ENST00000281043.3:c.847_849del ENSP00000281043.3:p.Glu283del
NM_001293228.1:c.847_849del NP_001280157.1:p.Glu283del
NM_001293231.1:c.214_216del NP_001280160.1:p.Glu72del
NM_001293233.1:c.*782_*784del NP_001280162.1:n.*782_*784del
NM_005378.5:c.847_849del NP_005369.2:p.Glu283del
NM_005378.6:c.847_849del MANE Select NP_005369.2:p.Glu283del
NM_001293228.2:c.847_849del NP_001280157.1:p.Glu283del
NM_001293231.2:c.214_216del NP_001280160.1:p.Glu72del
NM_001293233.2:c.*782_*784del NP_001280162.1:n.*782_*784del