Canonical Allele Identifier: CA847209325

Gene: MYC

Linked Data

• dbSNP Id: rs1274246760
• gnomAD v4: 8-127738515-GACA-G
• MyVariant Identifiers: chr8:g.128750762_128750764del (hg19) ; chr8:g.127738516_127738518del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738518_127738520del , CM000670.2:g.127738518_127738520del	GRCh38
NC_000008.10:g.128750764_128750766del , CM000670.1:g.128750764_128750766del	GRCh37
NC_000008.9:g.128819946_128819948del	NCBI36
NG_007161.1:g.7449_7451del
NG_007161.2:g.8085_8087del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.256_258del	ENSP00000516742.1:p.Asn86del
ENST00000707114.1:c.256_258del	ENSP00000516743.1:p.Asn86del
ENST00000707115.1:c.256_258del	ENSP00000516744.1:p.Asn86del
ENST00000707116.1:c.256_258del	ENSP00000516745.1:p.Asn86del
ENST00000517291.2:c.298_300del	ENSP00000429441.2:p.Asn100del
ENST00000524013.2:c.298_300del	ENSP00000430235.2:p.Asn100del
ENST00000621592.8:c.301_303del MANE Select	ENSP00000478887.2:p.Asn101del
ENST00000651626.1:c.-45_-43del	ENSP00000499182.1:n.-45_-43del
ENST00000652288.1:c.256_258del	ENSP00000499105.1:p.Asn86del
ENST00000259523.10:c.256_258del	ENSP00000259523.6:p.Asn86del
ENST00000377970.6:c.256_258del	ENSP00000367207.3:p.Asn86del
ENST00000517291.1:c.298_300del	ENSP00000429441.1:p.Asn100del
ENST00000524013.1:c.298_300del	ENSP00000430235.1:p.Asn100del
ENST00000613283.1:c.301_303del	ENSP00000479618.1:p.Asn101del
ENST00000621592.5:c.301_303del	ENSP00000478887.1:p.Asn101del
NM_002467.4:c.301_303del	NP_002458.2:p.Asn101del
NM_001354870.1:c.298_300del	NP_001341799.1:p.Asn100del
NM_002467.5:c.301_303del	NP_002458.2:p.Asn101del
NM_002467.6:c.301_303del MANE Select	NP_002458.2:p.Asn101del