Canonical Allele Identifier: CA1119019334

Gene: MYC

Linked Data

• dbSNP Id: rs1813645768
• gnomAD v3: 8-127738479-TC-T
• gnomAD v4: 8-127738479-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738481del , CM000670.2:g.127738481del	GRCh38
NC_000008.10:g.128750727del , CM000670.1:g.128750727del	GRCh37
NC_000008.9:g.128819909del	NCBI36
NG_007161.1:g.7412del
NG_007161.2:g.8048del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.219del	ENSP00000516742.1:p.Tyr74ThrfsTer29
ENST00000707114.1:c.219del	ENSP00000516743.1:p.Tyr74ThrfsTer29
ENST00000707115.1:c.219del	ENSP00000516744.1:p.Tyr74ThrfsTer29
ENST00000707116.1:c.219del	ENSP00000516745.1:p.Tyr74ThrfsTer29
ENST00000517291.2:c.261del	ENSP00000429441.2:p.Tyr88ThrfsTer29
ENST00000524013.2:c.261del	ENSP00000430235.2:p.Tyr88ThrfsTer29
ENST00000621592.8:c.264del MANE Select	ENSP00000478887.2:p.Tyr89ThrfsTer29
ENST00000651626.1:c.-82del	ENSP00000499182.1:n.-82del
ENST00000652288.1:c.219del	ENSP00000499105.1:p.Tyr74ThrfsTer29
ENST00000259523.10:c.219del	ENSP00000259523.6:p.Tyr74ThrfsTer29
ENST00000377970.6:c.219del	ENSP00000367207.3:p.Tyr74ThrfsTer29
ENST00000517291.1:c.261del	ENSP00000429441.1:p.Tyr88ThrfsTer29
ENST00000524013.1:c.261del	ENSP00000430235.1:p.Tyr88ThrfsTer29
ENST00000613283.1:c.264del	ENSP00000479618.1:p.Tyr89ThrfsTer29
ENST00000621592.5:c.264del	ENSP00000478887.1:p.Tyr89ThrfsTer29
NM_002467.4:c.264del	NP_002458.2:p.Tyr89ThrfsTer29
NM_001354870.1:c.261del	NP_001341799.1:p.Tyr88ThrfsTer29
NM_002467.5:c.264del	NP_002458.2:p.Tyr89ThrfsTer29
NM_002467.6:c.264del MANE Select	NP_002458.2:p.Tyr89ThrfsTer29