Canonical Allele Identifier: CA4875228

Gene: MYC

Linked Data

• dbSNP Id: rs776242757
• ExAC: 8:128750586 CGAG / C
• gnomAD v2: 8-128750586-CGAG-C
• gnomAD v3: 8-127738340-CGAG-C
• gnomAD v4: 8-127738340-CGAG-C
• MyVariant Identifiers: chr8:g.128750587_128750589del (hg19) ; chr8:g.127738342_127738344del (hg38) ; chr8:g.127738341_127738343del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738347_127738349del , CM000670.2:g.127738347_127738349del	GRCh38
NC_000008.10:g.128750593_128750595del , CM000670.1:g.128750593_128750595del	GRCh37
NC_000008.9:g.128819775_128819777del	NCBI36
NG_007161.1:g.7278_7280del
NG_007161.2:g.7914_7916del

Transcript Alleles

HGVS	Amino-acid change
ENST00000707113.1:c.85_87del	ENSP00000516742.1:p.Glu29del
ENST00000707114.1:c.85_87del	ENSP00000516743.1:p.Glu29del
ENST00000707115.1:c.85_87del	ENSP00000516744.1:p.Glu29del
ENST00000707116.1:c.85_87del	ENSP00000516745.1:p.Glu29del
ENST00000517291.2:c.127_129del	ENSP00000429441.2:p.Glu43del
ENST00000524013.2:c.127_129del	ENSP00000430235.2:p.Glu43del
ENST00000621592.8:c.130_132del MANE Select	ENSP00000478887.2:p.Glu44del
ENST00000651626.1:c.-216_-214del	ENSP00000499182.1:n.-216_-214del
ENST00000652288.1:c.85_87del	ENSP00000499105.1:p.Glu29del
ENST00000259523.10:c.85_87del	ENSP00000259523.6:p.Glu29del
ENST00000377970.6:c.85_87del	ENSP00000367207.3:p.Glu29del
ENST00000517291.1:c.127_129del	ENSP00000429441.1:p.Glu43del
ENST00000520751.1:c.51_53del	ENSP00000430226.1:p.Arg18del
ENST00000524013.1:c.127_129del	ENSP00000430235.1:p.Glu43del
ENST00000613283.1:c.130_132del	ENSP00000479618.1:p.Glu44del
ENST00000621592.5:c.130_132del	ENSP00000478887.1:p.Glu44del
NM_002467.4:c.130_132del	NP_002458.2:p.Glu44del
NM_001354870.1:c.127_129del	NP_001341799.1:p.Glu43del
NM_002467.5:c.130_132del	NP_002458.2:p.Glu44del
NM_002467.6:c.130_132del MANE Select	NP_002458.2:p.Glu44del