Canonical Allele Identifier: CA1818466188
Gene: MYC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738300A= , CM000670.2:g.127738300A= GRCh38
NC_000008.10:g.128750546A= , CM000670.1:g.128750546A= GRCh37
NC_000008.9:g.128819728A= NCBI36
NG_007161.1:g.7231A=
NG_007161.2:g.7867A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.38A= ENSP00000516742.1:p.Asp13=
ENST00000707114.1:c.38A= ENSP00000516743.1:p.Asp13=
ENST00000707115.1:c.38A= ENSP00000516744.1:p.Asp13=
ENST00000707116.1:c.38A= ENSP00000516745.1:p.Asp13=
ENST00000517291.2:c.80A= ENSP00000429441.2:p.Asp27=
ENST00000524013.2:c.80A= ENSP00000430235.2:p.Asp27=
ENST00000621592.8:c.83A= MANE Select ENSP00000478887.2:p.Asp28=
ENST00000651626.1:c.-263A= ENSP00000499182.1:n.-263A=
ENST00000652288.1:c.38A= ENSP00000499105.1:p.Asp13=
ENST00000259523.10:c.38A= ENSP00000259523.6:p.Asp13=
ENST00000377970.6:c.38A= ENSP00000367207.3:p.Asp13=
ENST00000517291.1:c.80A= ENSP00000429441.1:p.Asp27=
ENST00000520751.1:c.4A= ENSP00000430226.1:p.Thr2=
ENST00000524013.1:c.80A= ENSP00000430235.1:p.Asp27=
ENST00000613283.1:c.83A= ENSP00000479618.1:p.Asp28=
ENST00000621592.5:c.83A= ENSP00000478887.1:p.Asp28=
NM_002467.4:c.83A= NP_002458.2:p.Asp28=
NM_001354870.1:c.80A= NP_001341799.1:p.Asp27=
NM_002467.5:c.83A= NP_002458.2:p.Asp28=
NM_002467.6:c.83A= MANE Select NP_002458.2:p.Asp28=