Canonical Allele Identifier: CA372279227

Gene: MYC

Linked Data

• MyVariant Identifiers: chr8:g.128750530A>G (hg19) ; chr8:g.127738284A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738284A>G , CM000670.2:g.127738284A>G	GRCh38
NC_000008.10:g.128750530A>G , CM000670.1:g.128750530A>G	GRCh37
NC_000008.9:g.128819712A>G	NCBI36
NG_007161.1:g.7215A>G
NG_007161.2:g.7851A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.22A>G	ENSP00000516742.1:p.Thr8Ala
ENST00000707114.1:c.22A>G	ENSP00000516743.1:p.Thr8Ala
ENST00000707115.1:c.22A>G	ENSP00000516744.1:p.Thr8Ala
ENST00000707116.1:c.22A>G	ENSP00000516745.1:p.Thr8Ala
ENST00000517291.2:c.64A>G	ENSP00000429441.2:p.Thr22Ala
ENST00000524013.2:c.64A>G	ENSP00000430235.2:p.Thr22Ala
ENST00000621592.8:c.67A>G MANE Select	ENSP00000478887.2:p.Thr23Ala
ENST00000651626.1:c.-279A>G	ENSP00000499182.1:n.-279A>G
ENST00000652288.1:c.22A>G	ENSP00000499105.1:p.Thr8Ala
ENST00000259523.10:c.22A>G	ENSP00000259523.6:p.Thr8Ala
ENST00000377970.6:c.22A>G	ENSP00000367207.3:p.Thr8Ala
ENST00000517291.1:c.64A>G	ENSP00000429441.1:p.Thr22Ala
ENST00000520751.1:c.-5-8A>G	ENSP00000430226.1:n.-5-8A>G
ENST00000524013.1:c.64A>G	ENSP00000430235.1:p.Thr22Ala
ENST00000613283.1:c.67A>G	ENSP00000479618.1:p.Thr23Ala
ENST00000621592.5:c.67A>G	ENSP00000478887.1:p.Thr23Ala
NM_002467.4:c.67A>G	NP_002458.2:p.Thr23Ala
NM_001354870.1:c.64A>G	NP_001341799.1:p.Thr22Ala
NM_002467.5:c.67A>G	NP_002458.2:p.Thr23Ala
NM_002467.6:c.67A>G MANE Select	NP_002458.2:p.Thr23Ala