Canonical Allele Identifier: CA1818466045

Gene: MYC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738213_127738215delinsCAA , CM000670.2:g.127738213_127738215delinsCAA	GRCh38
NC_000008.10:g.128750459_128750461delinsCAA , CM000670.1:g.128750459_128750461delinsCAA	GRCh37
NC_000008.9:g.128819641_128819643delinsCAA	NCBI36
NG_007161.1:g.7144_7146delinsCAA
NG_007161.2:g.7780_7782delinsCAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.-15-35_-15-33delinsCAA	ENSP00000516742.1:n.-15-35_-15-33delinsCAA
ENST00000707114.1:c.-15-35_-15-33delinsCAA	ENSP00000516743.1:n.-15-35_-15-33delinsCAA
ENST00000707115.1:c.-50_-48delinsCAA	ENSP00000516744.1:n.-50_-48delinsCAA
ENST00000707116.1:c.-15-35_-15-33delinsCAA	ENSP00000516745.1:n.-15-35_-15-33delinsCAA
ENST00000517291.2:c.31-38_31-36delinsCAA	ENSP00000429441.2:n.31-38_31-36delinsCAA
ENST00000524013.2:c.31-38_31-36delinsCAA	ENSP00000430235.2:n.31-38_31-36delinsCAA
ENST00000621592.8:c.31-35_31-33delinsCAA MANE Select	ENSP00000478887.2:n.31-35_31-33delinsCAA
ENST00000651626.1:c.-283-67_-283-65delinsCAA	ENSP00000499182.1:n.-283-67_-283-65delinsCAA
ENST00000652288.1:c.-15-35_-15-33delinsCAA	ENSP00000499105.1:n.-15-35_-15-33delinsCAA
ENST00000259523.10:c.-15-35_-15-33delinsCAA	ENSP00000259523.6:n.-15-35_-15-33delinsCAA
ENST00000377970.6:c.-15-35_-15-33delinsCAA	ENSP00000367207.3:n.-15-35_-15-33delinsCAA
ENST00000517291.1:c.31-38_31-36delinsCAA	ENSP00000429441.1:n.31-38_31-36delinsCAA
ENST00000520751.1:c.-5-79_-5-77delinsCAA	ENSP00000430226.1:n.-5-79_-5-77delinsCAA
ENST00000524013.1:c.31-38_31-36delinsCAA	ENSP00000430235.1:n.31-38_31-36delinsCAA
ENST00000613283.1:c.31-35_31-33delinsCAA	ENSP00000479618.1:n.31-35_31-33delinsCAA
ENST00000621592.5:c.31-35_31-33delinsCAA	ENSP00000478887.1:n.31-35_31-33delinsCAA
NM_002467.4:c.31-35_31-33delinsCAA	NP_002458.2:n.31-35_31-33delinsCAA
NM_001354870.1:c.31-38_31-36delinsCAA	NP_001341799.1:n.31-38_31-36delinsCAA
NM_002467.5:c.31-35_31-33delinsCAA	NP_002458.2:n.31-35_31-33delinsCAA
NM_002467.6:c.31-35_31-33delinsCAA MANE Select	NP_002458.2:n.31-35_31-33delinsCAA