Canonical Allele Identifier: CA1818466186

Gene: MYC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738296T= , CM000670.2:g.127738296T=	GRCh38
NC_000008.10:g.128750542T= , CM000670.1:g.128750542T=	GRCh37
NC_000008.9:g.128819724T=	NCBI36
NG_007161.1:g.7227T=
NG_007161.2:g.7863T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.34T=	ENSP00000516742.1:p.Tyr12=
ENST00000707114.1:c.34T=	ENSP00000516743.1:p.Tyr12=
ENST00000707115.1:c.34T=	ENSP00000516744.1:p.Tyr12=
ENST00000707116.1:c.34T=	ENSP00000516745.1:p.Tyr12=
ENST00000517291.2:c.76T=	ENSP00000429441.2:p.Tyr26=
ENST00000524013.2:c.76T=	ENSP00000430235.2:p.Tyr26=
ENST00000621592.8:c.79T= MANE Select	ENSP00000478887.2:p.Tyr27=
ENST00000651626.1:c.-267T=	ENSP00000499182.1:n.-267T=
ENST00000652288.1:c.34T=	ENSP00000499105.1:p.Tyr12=
ENST00000259523.10:c.34T=	ENSP00000259523.6:p.Tyr12=
ENST00000377970.6:c.34T=	ENSP00000367207.3:p.Tyr12=
ENST00000517291.1:c.76T=	ENSP00000429441.1:p.Tyr26=
ENST00000520751.1:c.-1T=	ENSP00000430226.1:n.-1T=
ENST00000524013.1:c.76T=	ENSP00000430235.1:p.Tyr26=
ENST00000613283.1:c.79T=	ENSP00000479618.1:p.Tyr27=
ENST00000621592.5:c.79T=	ENSP00000478887.1:p.Tyr27=
NM_002467.4:c.79T=	NP_002458.2:p.Tyr27=
NM_001354870.1:c.76T=	NP_001341799.1:p.Tyr26=
NM_002467.5:c.79T=	NP_002458.2:p.Tyr27=
NM_002467.6:c.79T= MANE Select	NP_002458.2:p.Tyr27=