Canonical Allele Identifier: CA1818466365
Gene: MYC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738386C= , CM000670.2:g.127738386C= GRCh38
NC_000008.10:g.128750632C= , CM000670.1:g.128750632C= GRCh37
NC_000008.9:g.128819814C= NCBI36
NG_007161.1:g.7317C=
NG_007161.2:g.7953C=

Transcript Alleles

HGVS Amino-acid change
ENST00000707113.1:c.124C= ENSP00000516742.1:p.Pro42=
ENST00000707114.1:c.124C= ENSP00000516743.1:p.Pro42=
ENST00000707115.1:c.124C= ENSP00000516744.1:p.Pro42=
ENST00000707116.1:c.124C= ENSP00000516745.1:p.Pro42=
ENST00000517291.2:c.166C= ENSP00000429441.2:p.Pro56=
ENST00000524013.2:c.166C= ENSP00000430235.2:p.Pro56=
ENST00000621592.8:c.169C= MANE Select ENSP00000478887.2:p.Pro57=
ENST00000651626.1:c.-177C= ENSP00000499182.1:n.-177C=
ENST00000652288.1:c.124C= ENSP00000499105.1:p.Pro42=
ENST00000259523.10:c.124C= ENSP00000259523.6:p.Pro42=
ENST00000377970.6:c.124C= ENSP00000367207.3:p.Pro42=
ENST00000517291.1:c.166C= ENSP00000429441.1:p.Pro56=
ENST00000520751.1:c.90C= ENSP00000430226.1:p.Ser30=
ENST00000524013.1:c.166C= ENSP00000430235.1:p.Pro56=
ENST00000613283.1:c.169C= ENSP00000479618.1:p.Pro57=
ENST00000621592.5:c.169C= ENSP00000478887.1:p.Pro57=
NM_002467.4:c.169C= NP_002458.2:p.Pro57=
NM_001354870.1:c.166C= NP_001341799.1:p.Pro56=
NM_002467.5:c.169C= NP_002458.2:p.Pro57=
NM_002467.6:c.169C= MANE Select NP_002458.2:p.Pro57=