Canonical Allele Identifier: CA341314
Gene: MYCN HGNC NCBI
MYCNOS HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.15942281G>T , CM000664.2:g.15942281G>T GRCh38
NC_000002.11:g.16082403G>T , CM000664.1:g.16082403G>T GRCh37
NC_000002.10:g.15999854G>T NCBI36
NG_007457.1:g.6721G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000281043.4:c.217G>T (MYCN) MANE Select ENSP00000281043.3:p.Glu73Ter
ENST00000638417.1:c.157+1538G>T (MYCN) ENSP00000491476.1:n.157+1538G>T
ENST00000281043.3:c.217G>T (MYCN) ENSP00000281043.3:p.Glu73Ter
NM_001293228.1:c.217G>T (MYCN) NP_001280157.1:p.Glu73Ter
NM_001293231.1:c.157+1538G>T (MYCN) NP_001280160.1:n.157+1538G>T
NM_001293233.1:c.*152G>T (MYCN) NP_001280162.1:n.*152G>T
NM_005378.5:c.217G>T (MYCN) NP_005369.2:p.Glu73Ter
XM_024452528.1:c.-234+101C>A (MYCNOS) XP_024308296.1:n.-234+101C>A
NM_005378.6:c.217G>T (MYCN) MANE Select NP_005369.2:p.Glu73Ter
NM_001293228.2:c.217G>T (MYCN) NP_001280157.1:p.Glu73Ter
NM_001293231.2:c.157+1538G>T (MYCN) NP_001280160.1:n.157+1538G>T
NM_001293233.2:c.*152G>T (MYCN) NP_001280162.1:n.*152G>T
NR_161163.1:n.153C>A (MYCNOS)
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