Canonical Allele Identifier: CA645565238
Gene: MYC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738435_127738443del , CM000670.2:g.127738435_127738443del GRCh38
NC_000008.10:g.128750681_128750689del , CM000670.1:g.128750681_128750689del GRCh37
NC_000008.9:g.128819863_128819871del NCBI36
NG_007161.1:g.7366_7374del
NG_007161.2:g.8002_8010del

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.173_181del ENSP00000516742.1:p.Thr58_Leu61delinsMet
ENST00000707114.1:c.173_181del ENSP00000516743.1:p.Thr58_Leu61delinsMet
ENST00000707115.1:c.173_181del ENSP00000516744.1:p.Thr58_Leu61delinsMet
ENST00000707116.1:c.173_181del ENSP00000516745.1:p.Thr58_Leu61delinsMet
ENST00000517291.2:c.215_223del ENSP00000429441.2:p.Thr72_Leu75delinsMet
ENST00000524013.2:c.215_223del ENSP00000430235.2:p.Thr72_Leu75delinsMet
ENST00000621592.8:c.218_226del MANE Select ENSP00000478887.2:p.Thr73_Leu76delinsMet
ENST00000651626.1:c.-128_-120del ENSP00000499182.1:n.-128_-120del
ENST00000652288.1:c.173_181del ENSP00000499105.1:p.Thr58_Leu61delinsMet
ENST00000259523.10:c.173_181del ENSP00000259523.6:p.Thr58_Leu61delinsMet
ENST00000377970.6:c.173_181del ENSP00000367207.3:p.Thr58_Leu61delinsMet
ENST00000517291.1:c.215_223del ENSP00000429441.1:p.Thr72_Leu75delinsMet
ENST00000520751.1:c.139_147del ENSP00000430226.1:p.Pro47_Pro49del
ENST00000524013.1:c.215_223del ENSP00000430235.1:p.Thr72_Leu75delinsMet
ENST00000613283.1:c.218_226del ENSP00000479618.1:p.Thr73_Leu76delinsMet
ENST00000621592.5:c.218_226del ENSP00000478887.1:p.Thr73_Leu76delinsMet
NM_002467.4:c.218_226del NP_002458.2:p.Thr73_Leu76delinsMet
NM_001354870.1:c.215_223del NP_001341799.1:p.Thr72_Leu75delinsMet
NM_002467.5:c.218_226del NP_002458.2:p.Thr73_Leu76delinsMet
NM_002467.6:c.218_226del MANE Select NP_002458.2:p.Thr73_Leu76delinsMet