Canonical Allele Identifier: CA645565237
Gene: MYC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738431_127738433del , CM000670.2:g.127738431_127738433del GRCh38
NC_000008.10:g.128750677_128750679del , CM000670.1:g.128750677_128750679del GRCh37
NC_000008.9:g.128819859_128819861del NCBI36
NG_007161.1:g.7362_7364del
NG_007161.2:g.7998_8000del

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.169_171del ENSP00000516742.1:p.Pro57del
ENST00000707114.1:c.169_171del ENSP00000516743.1:p.Pro57del
ENST00000707115.1:c.169_171del ENSP00000516744.1:p.Pro57del
ENST00000707116.1:c.169_171del ENSP00000516745.1:p.Pro57del
ENST00000517291.2:c.211_213del ENSP00000429441.2:p.Pro71del
ENST00000524013.2:c.211_213del ENSP00000430235.2:p.Pro71del
ENST00000621592.8:c.214_216del MANE Select ENSP00000478887.2:p.Pro72del
ENST00000651626.1:c.-132_-130del ENSP00000499182.1:n.-132_-130del
ENST00000652288.1:c.169_171del ENSP00000499105.1:p.Pro57del
ENST00000259523.10:c.169_171del ENSP00000259523.6:p.Pro57del
ENST00000377970.6:c.169_171del ENSP00000367207.3:p.Pro57del
ENST00000517291.1:c.211_213del ENSP00000429441.1:p.Pro71del
ENST00000520751.1:c.135_137del ENSP00000430226.1:p.Cys45Ter
ENST00000524013.1:c.211_213del ENSP00000430235.1:p.Pro71del
ENST00000613283.1:c.214_216del ENSP00000479618.1:p.Pro72del
ENST00000621592.5:c.214_216del ENSP00000478887.1:p.Pro72del
NM_002467.4:c.214_216del NP_002458.2:p.Pro72del
NM_001354870.1:c.211_213del NP_001341799.1:p.Pro71del
NM_002467.5:c.214_216del NP_002458.2:p.Pro72del
NM_002467.6:c.214_216del MANE Select NP_002458.2:p.Pro72del