Canonical Allele Identifier: CA372279466
Gene: MYC HGNC NCBI

Linked Data

dbSNP Id: rs1329377103

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738372A>T , CM000670.2:g.127738372A>T GRCh38
NC_000008.10:g.128750618A>T , CM000670.1:g.128750618A>T GRCh37
NC_000008.9:g.128819800A>T NCBI36
NG_007161.1:g.7303A>T
NG_007161.2:g.7939A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.110A>T ENSP00000516742.1:p.Gln37Leu
ENST00000707114.1:c.110A>T ENSP00000516743.1:p.Gln37Leu
ENST00000707115.1:c.110A>T ENSP00000516744.1:p.Gln37Leu
ENST00000707116.1:c.110A>T ENSP00000516745.1:p.Gln37Leu
ENST00000517291.2:c.152A>T ENSP00000429441.2:p.Gln51Leu
ENST00000524013.2:c.152A>T ENSP00000430235.2:p.Gln51Leu
ENST00000621592.8:c.155A>T MANE Select ENSP00000478887.2:p.Gln52Leu
ENST00000651626.1:c.-191A>T ENSP00000499182.1:n.-191A>T
ENST00000652288.1:c.110A>T ENSP00000499105.1:p.Gln37Leu
ENST00000259523.10:c.110A>T ENSP00000259523.6:p.Gln37Leu
ENST00000377970.6:c.110A>T ENSP00000367207.3:p.Gln37Leu
ENST00000517291.1:c.152A>T ENSP00000429441.1:p.Gln51Leu
ENST00000520751.1:c.76A>T ENSP00000430226.1:p.Arg26Ter
ENST00000524013.1:c.152A>T ENSP00000430235.1:p.Gln51Leu
ENST00000613283.1:c.155A>T ENSP00000479618.1:p.Gln52Leu
ENST00000621592.5:c.155A>T ENSP00000478887.1:p.Gln52Leu
NM_002467.4:c.155A>T NP_002458.2:p.Gln52Leu
NM_001354870.1:c.152A>T NP_001341799.1:p.Gln51Leu
NM_002467.5:c.155A>T NP_002458.2:p.Gln52Leu
NM_002467.6:c.155A>T MANE Select NP_002458.2:p.Gln52Leu