Canonical Allele Identifier: CA2573332252

Gene: MYC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738436_127738438del , CM000670.2:g.127738436_127738438del	GRCh38
NC_000008.10:g.128750682_128750684del , CM000670.1:g.128750682_128750684del	GRCh37
NC_000008.9:g.128819864_128819866del	NCBI36
NG_007161.1:g.7367_7369del
NG_007161.2:g.8003_8005del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.174_176del	ENSP00000516742.1:p.Pro59del
ENST00000707114.1:c.174_176del	ENSP00000516743.1:p.Pro59del
ENST00000707115.1:c.174_176del	ENSP00000516744.1:p.Pro59del
ENST00000707116.1:c.174_176del	ENSP00000516745.1:p.Pro59del
ENST00000517291.2:c.216_218del	ENSP00000429441.2:p.Pro73del
ENST00000524013.2:c.216_218del	ENSP00000430235.2:p.Pro73del
ENST00000621592.8:c.219_221del MANE Select	ENSP00000478887.2:p.Pro74del
ENST00000651626.1:c.-127_-125del	ENSP00000499182.1:n.-127_-125del
ENST00000652288.1:c.174_176del	ENSP00000499105.1:p.Pro59del
ENST00000259523.10:c.174_176del	ENSP00000259523.6:p.Pro59del
ENST00000377970.6:c.174_176del	ENSP00000367207.3:p.Pro59del
ENST00000517291.1:c.216_218del	ENSP00000429441.1:p.Pro73del
ENST00000520751.1:c.140_142del	ENSP00000430226.1:p.Pro47del
ENST00000524013.1:c.216_218del	ENSP00000430235.1:p.Pro73del
ENST00000613283.1:c.219_221del	ENSP00000479618.1:p.Pro74del
ENST00000621592.5:c.219_221del	ENSP00000478887.1:p.Pro74del
NM_002467.4:c.219_221del	NP_002458.2:p.Pro74del
NM_001354870.1:c.216_218del	NP_001341799.1:p.Pro73del
NM_002467.5:c.219_221del	NP_002458.2:p.Pro74del
NM_002467.6:c.219_221del MANE Select	NP_002458.2:p.Pro74del