Canonical Allele Identifier: CA4875235

Gene: MYC

Linked Data

• dbSNP Id: rs745729043
• ExAC: 8:128750604 C / CCAG
• gnomAD v2: 8-128750604-C-CCAG
• gnomAD v3: 8-127738358-C-CCAG
• gnomAD v4: 8-127738358-C-CCAG
• MyVariant Identifiers: chr8:g.128750607_128750608insCAG (hg19) ; chr8:g.128750604_128750605insCAG (hg19) ; chr8:g.127738361_127738362insCAG (hg38) ; chr8:g.127738358_127738359insCAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738371_127738373dup , CM000670.2:g.127738371_127738373dup	GRCh38
NC_000008.10:g.128750617_128750619dup , CM000670.1:g.128750617_128750619dup	GRCh37
NC_000008.9:g.128819799_128819801dup	NCBI36
NG_007161.1:g.7302_7304dup
NG_007161.2:g.7938_7940dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.109_111dup	ENSP00000516742.1:p.Gln37_Ser38insGln
ENST00000707114.1:c.109_111dup	ENSP00000516743.1:p.Gln37_Ser38insGln
ENST00000707115.1:c.109_111dup	ENSP00000516744.1:p.Gln37_Ser38insGln
ENST00000707116.1:c.109_111dup	ENSP00000516745.1:p.Gln37_Ser38insGln
ENST00000517291.2:c.151_153dup	ENSP00000429441.2:p.Gln51_Ser52insGln
ENST00000524013.2:c.151_153dup	ENSP00000430235.2:p.Gln51_Ser52insGln
ENST00000621592.8:c.154_156dup MANE Select	ENSP00000478887.2:p.Gln52_Ser53insGln
ENST00000651626.1:c.-192_-190dup	ENSP00000499182.1:n.-192_-190dup
ENST00000652288.1:c.109_111dup	ENSP00000499105.1:p.Gln37_Ser38insGln
ENST00000259523.10:c.109_111dup	ENSP00000259523.6:p.Gln37_Ser38insGln
ENST00000377970.6:c.109_111dup	ENSP00000367207.3:p.Gln37_Ser38insGln
ENST00000517291.1:c.151_153dup	ENSP00000429441.1:p.Gln51_Ser52insGln
ENST00000520751.1:c.75_77dup	ENSP00000430226.1:p.Ser25_Arg26insSer
ENST00000524013.1:c.151_153dup	ENSP00000430235.1:p.Gln51_Ser52insGln
ENST00000613283.1:c.154_156dup	ENSP00000479618.1:p.Gln52_Ser53insGln
ENST00000621592.5:c.154_156dup	ENSP00000478887.1:p.Gln52_Ser53insGln
NM_002467.4:c.154_156dup	NP_002458.2:p.Gln52_Ser53insGln
NM_001354870.1:c.151_153dup	NP_001341799.1:p.Gln51_Ser52insGln
NM_002467.5:c.154_156dup	NP_002458.2:p.Gln52_Ser53insGln
NM_002467.6:c.154_156dup MANE Select	NP_002458.2:p.Gln52_Ser53insGln