Canonical Allele Identifier: CA2688552186

Gene: MYC

Linked Data

• gnomAD v4: 8-127738385-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738390del , CM000670.2:g.127738390del	GRCh38
NC_000008.10:g.128750636del , CM000670.1:g.128750636del	GRCh37
NC_000008.9:g.128819818del	NCBI36
NG_007161.1:g.7321del
NG_007161.2:g.7957del

Transcript Alleles

HGVS	Amino-acid change
ENST00000707113.1:c.128del	ENSP00000516742.1:p.Pro43ArgfsTer?
ENST00000707114.1:c.128del	ENSP00000516743.1:p.Pro43ArgfsTer?
ENST00000707115.1:c.128del	ENSP00000516744.1:p.Pro43ArgfsTer?
ENST00000707116.1:c.128del	ENSP00000516745.1:p.Pro43ArgfsTer?
ENST00000517291.2:c.170del	ENSP00000429441.2:p.Pro57ArgfsTer?
ENST00000524013.2:c.170del	ENSP00000430235.2:p.Pro57ArgfsTer?
ENST00000621592.8:c.173del MANE Select	ENSP00000478887.2:p.Pro58ArgfsTer?
ENST00000651626.1:c.-173del	ENSP00000499182.1:n.-173del
ENST00000652288.1:c.128del	ENSP00000499105.1:p.Pro43ArgfsTer?
ENST00000259523.10:c.128del	ENSP00000259523.6:p.Pro43ArgfsTer?
ENST00000377970.6:c.128del	ENSP00000367207.3:p.Pro43ArgfsTer?
ENST00000517291.1:c.170del	ENSP00000429441.1:p.Pro57ArgfsTer?
ENST00000520751.1:c.94del	ENSP00000430226.1:p.Arg32GlyfsTer21
ENST00000524013.1:c.170del	ENSP00000430235.1:p.Pro57ArgfsTer?
ENST00000613283.1:c.173del	ENSP00000479618.1:p.Pro58ArgfsTer?
ENST00000621592.5:c.173del	ENSP00000478887.1:p.Pro58ArgfsTer?
NM_002467.4:c.173del	NP_002458.2:p.Pro58ArgfsTer?
NM_001354870.1:c.170del	NP_001341799.1:p.Pro57ArgfsTer?
NM_002467.5:c.173del	NP_002458.2:p.Pro58ArgfsTer?
NM_002467.6:c.173del MANE Select	NP_002458.2:p.Pro58ArgfsTer?