Canonical Allele Identifier: CA1818466397
Gene: MYC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738403G= , CM000670.2:g.127738403G= GRCh38
NC_000008.10:g.128750649G= , CM000670.1:g.128750649G= GRCh37
NC_000008.9:g.128819831G= NCBI36
NG_007161.1:g.7334G=
NG_007161.2:g.7970G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.141G= ENSP00000516742.1:p.Glu47=
ENST00000707114.1:c.141G= ENSP00000516743.1:p.Glu47=
ENST00000707115.1:c.141G= ENSP00000516744.1:p.Glu47=
ENST00000707116.1:c.141G= ENSP00000516745.1:p.Glu47=
ENST00000517291.2:c.183G= ENSP00000429441.2:p.Glu61=
ENST00000524013.2:c.183G= ENSP00000430235.2:p.Glu61=
ENST00000621592.8:c.186G= MANE Select ENSP00000478887.2:p.Glu62=
ENST00000651626.1:c.-160G= ENSP00000499182.1:n.-160G=
ENST00000652288.1:c.141G= ENSP00000499105.1:p.Glu47=
ENST00000259523.10:c.141G= ENSP00000259523.6:p.Glu47=
ENST00000377970.6:c.141G= ENSP00000367207.3:p.Glu47=
ENST00000517291.1:c.183G= ENSP00000429441.1:p.Glu61=
ENST00000520751.1:c.107G= ENSP00000430226.1:p.Arg36=
ENST00000524013.1:c.183G= ENSP00000430235.1:p.Glu61=
ENST00000613283.1:c.186G= ENSP00000479618.1:p.Glu62=
ENST00000621592.5:c.186G= ENSP00000478887.1:p.Glu62=
NM_002467.4:c.186G= NP_002458.2:p.Glu62=
NM_001354870.1:c.183G= NP_001341799.1:p.Glu61=
NM_002467.5:c.186G= NP_002458.2:p.Glu62=
NM_002467.6:c.186G= MANE Select NP_002458.2:p.Glu62=