Canonical Allele Identifier: CA1818466399
Gene: MYC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738405A= , CM000670.2:g.127738405A= GRCh38
NC_000008.10:g.128750651A= , CM000670.1:g.128750651A= GRCh37
NC_000008.9:g.128819833A= NCBI36
NG_007161.1:g.7336A=
NG_007161.2:g.7972A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.143A= ENSP00000516742.1:p.Asp48=
ENST00000707114.1:c.143A= ENSP00000516743.1:p.Asp48=
ENST00000707115.1:c.143A= ENSP00000516744.1:p.Asp48=
ENST00000707116.1:c.143A= ENSP00000516745.1:p.Asp48=
ENST00000517291.2:c.185A= ENSP00000429441.2:p.Asp62=
ENST00000524013.2:c.185A= ENSP00000430235.2:p.Asp62=
ENST00000621592.8:c.188A= MANE Select ENSP00000478887.2:p.Asp63=
ENST00000651626.1:c.-158A= ENSP00000499182.1:n.-158A=
ENST00000652288.1:c.143A= ENSP00000499105.1:p.Asp48=
ENST00000259523.10:c.143A= ENSP00000259523.6:p.Asp48=
ENST00000377970.6:c.143A= ENSP00000367207.3:p.Asp48=
ENST00000517291.1:c.185A= ENSP00000429441.1:p.Asp62=
ENST00000520751.1:c.109A= ENSP00000430226.1:p.Ile37=
ENST00000524013.1:c.185A= ENSP00000430235.1:p.Asp62=
ENST00000613283.1:c.188A= ENSP00000479618.1:p.Asp63=
ENST00000621592.5:c.188A= ENSP00000478887.1:p.Asp63=
NM_002467.4:c.188A= NP_002458.2:p.Asp63=
NM_001354870.1:c.185A= NP_001341799.1:p.Asp62=
NM_002467.5:c.188A= NP_002458.2:p.Asp63=
NM_002467.6:c.188A= MANE Select NP_002458.2:p.Asp63=