Canonical Allele Identifier: CA122524
Gene: MYC HGNC NCBI

Linked Data

ClinVar Variation Id: 12576
ClinVar RCV Id: RCV000013404
dbSNP Id: rs121918684

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738379G>C , CM000670.2:g.127738379G>C GRCh38
NC_000008.10:g.128750625G>C , CM000670.1:g.128750625G>C GRCh37
NC_000008.9:g.128819807G>C NCBI36
NG_007161.1:g.7310G>C
NG_007161.2:g.7946G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000707113.1:c.117G>C ENSP00000516742.1:p.Glu39Asp
ENST00000707114.1:c.117G>C ENSP00000516743.1:p.Glu39Asp
ENST00000707115.1:c.117G>C ENSP00000516744.1:p.Glu39Asp
ENST00000707116.1:c.117G>C ENSP00000516745.1:p.Glu39Asp
ENST00000517291.2:c.159G>C ENSP00000429441.2:p.Glu53Asp
ENST00000524013.2:c.159G>C ENSP00000430235.2:p.Glu53Asp
ENST00000621592.8:c.162G>C MANE Select ENSP00000478887.2:p.Glu54Asp
ENST00000651626.1:c.-184G>C ENSP00000499182.1:n.-184G>C
ENST00000652288.1:c.117G>C ENSP00000499105.1:p.Glu39Asp
ENST00000259523.10:c.117G>C ENSP00000259523.6:p.Glu39Asp
ENST00000377970.6:c.117G>C ENSP00000367207.3:p.Glu39Asp
ENST00000517291.1:c.159G>C ENSP00000429441.1:p.Glu53Asp
ENST00000520751.1:c.83G>C ENSP00000430226.1:p.Ser28Thr
ENST00000524013.1:c.159G>C ENSP00000430235.1:p.Glu53Asp
ENST00000613283.1:c.162G>C ENSP00000479618.1:p.Glu54Asp
ENST00000621592.5:c.162G>C ENSP00000478887.1:p.Glu54Asp
NM_002467.4:c.162G>C NP_002458.2:p.Glu54Asp
NM_001354870.1:c.159G>C NP_001341799.1:p.Glu53Asp
NM_002467.5:c.162G>C NP_002458.2:p.Glu54Asp
NM_002467.6:c.162G>C MANE Select NP_002458.2:p.Glu54Asp