Canonical Allele Identifier: CA1818466201
Gene: MYC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738305G= , CM000670.2:g.127738305G= GRCh38
NC_000008.10:g.128750551G= , CM000670.1:g.128750551G= GRCh37
NC_000008.9:g.128819733G= NCBI36
NG_007161.1:g.7236G=
NG_007161.2:g.7872G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.43G= ENSP00000516742.1:p.Asp15=
ENST00000707114.1:c.43G= ENSP00000516743.1:p.Asp15=
ENST00000707115.1:c.43G= ENSP00000516744.1:p.Asp15=
ENST00000707116.1:c.43G= ENSP00000516745.1:p.Asp15=
ENST00000517291.2:c.85G= ENSP00000429441.2:p.Asp29=
ENST00000524013.2:c.85G= ENSP00000430235.2:p.Asp29=
ENST00000621592.8:c.88G= MANE Select ENSP00000478887.2:p.Asp30=
ENST00000651626.1:c.-258G= ENSP00000499182.1:n.-258G=
ENST00000652288.1:c.43G= ENSP00000499105.1:p.Asp15=
ENST00000259523.10:c.43G= ENSP00000259523.6:p.Asp15=
ENST00000377970.6:c.43G= ENSP00000367207.3:p.Asp15=
ENST00000517291.1:c.85G= ENSP00000429441.1:p.Asp29=
ENST00000520751.1:c.9G= ENSP00000430226.1:p.Ser3=
ENST00000524013.1:c.85G= ENSP00000430235.1:p.Asp29=
ENST00000613283.1:c.88G= ENSP00000479618.1:p.Asp30=
ENST00000621592.5:c.88G= ENSP00000478887.1:p.Asp30=
NM_002467.4:c.88G= NP_002458.2:p.Asp30=
NM_001354870.1:c.85G= NP_001341799.1:p.Asp29=
NM_002467.5:c.88G= NP_002458.2:p.Asp30=
NM_002467.6:c.88G= MANE Select NP_002458.2:p.Asp30=