Canonical Allele Identifier: CA1818466546

Gene: MYC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738484C= , CM000670.2:g.127738484C=	GRCh38
NC_000008.10:g.128750730C= , CM000670.1:g.128750730C=	GRCh37
NC_000008.9:g.128819912C=	NCBI36
NG_007161.1:g.7415C=
NG_007161.2:g.8051C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.222C=	ENSP00000516742.1:p.Tyr74=
ENST00000707114.1:c.222C=	ENSP00000516743.1:p.Tyr74=
ENST00000707115.1:c.222C=	ENSP00000516744.1:p.Tyr74=
ENST00000707116.1:c.222C=	ENSP00000516745.1:p.Tyr74=
ENST00000517291.2:c.264C=	ENSP00000429441.2:p.Tyr88=
ENST00000524013.2:c.264C=	ENSP00000430235.2:p.Tyr88=
ENST00000621592.8:c.267C= MANE Select	ENSP00000478887.2:p.Tyr89=
ENST00000651626.1:c.-79C=	ENSP00000499182.1:n.-79C=
ENST00000652288.1:c.222C=	ENSP00000499105.1:p.Tyr74=
ENST00000259523.10:c.222C=	ENSP00000259523.6:p.Tyr74=
ENST00000377970.6:c.222C=	ENSP00000367207.3:p.Tyr74=
ENST00000517291.1:c.264C=	ENSP00000429441.1:p.Tyr88=
ENST00000524013.1:c.264C=	ENSP00000430235.1:p.Tyr88=
ENST00000613283.1:c.267C=	ENSP00000479618.1:p.Tyr89=
ENST00000621592.5:c.267C=	ENSP00000478887.1:p.Tyr89=
NM_002467.4:c.267C=	NP_002458.2:p.Tyr89=
NM_001354870.1:c.264C=	NP_001341799.1:p.Tyr88=
NM_002467.5:c.267C=	NP_002458.2:p.Tyr89=
NM_002467.6:c.267C= MANE Select	NP_002458.2:p.Tyr89=