Canonical Allele Identifier: CA372279370
Gene: MYC HGNC NCBI

Linked Data

dbSNP Id: rs2130092552

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738338G>A , CM000670.2:g.127738338G>A GRCh38
NC_000008.10:g.128750584G>A , CM000670.1:g.128750584G>A GRCh37
NC_000008.9:g.128819766G>A NCBI36
NG_007161.1:g.7269G>A
NG_007161.2:g.7905G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000707113.1:c.76G>A ENSP00000516742.1:p.Asp26Asn
ENST00000707114.1:c.76G>A ENSP00000516743.1:p.Asp26Asn
ENST00000707115.1:c.76G>A ENSP00000516744.1:p.Asp26Asn
ENST00000707116.1:c.76G>A ENSP00000516745.1:p.Asp26Asn
ENST00000517291.2:c.118G>A ENSP00000429441.2:p.Asp40Asn
ENST00000524013.2:c.118G>A ENSP00000430235.2:p.Asp40Asn
ENST00000621592.8:c.121G>A MANE Select ENSP00000478887.2:p.Asp41Asn
ENST00000651626.1:c.-225G>A ENSP00000499182.1:n.-225G>A
ENST00000652288.1:c.76G>A ENSP00000499105.1:p.Asp26Asn
ENST00000259523.10:c.76G>A ENSP00000259523.6:p.Asp26Asn
ENST00000377970.6:c.76G>A ENSP00000367207.3:p.Asp26Asn
ENST00000517291.1:c.118G>A ENSP00000429441.1:p.Asp40Asn
ENST00000520751.1:c.42G>A ENSP00000430226.1:p.Ala14=
ENST00000524013.1:c.118G>A ENSP00000430235.1:p.Asp40Asn
ENST00000613283.1:c.121G>A ENSP00000479618.1:p.Asp41Asn
ENST00000621592.5:c.121G>A ENSP00000478887.1:p.Asp41Asn
NM_002467.4:c.121G>A NP_002458.2:p.Asp41Asn
NM_001354870.1:c.118G>A NP_001341799.1:p.Asp40Asn
NM_002467.5:c.121G>A NP_002458.2:p.Asp41Asn
NM_002467.6:c.121G>A MANE Select NP_002458.2:p.Asp41Asn