Canonical Allele Identifier: CA372280842

Gene: MYC

Linked Data - Predicted Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738995C>A , CM000670.2:g.127738995C>A	GRCh38
NC_000008.10:g.128751241C>A , CM000670.1:g.128751241C>A	GRCh37
NC_000008.9:g.128820423C>A	NCBI36
NG_007161.1:g.7926C>A
NG_007161.2:g.8562C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.733C>A	ENSP00000516742.1:p.Pro245Thr
ENST00000707114.1:c.733C>A	ENSP00000516743.1:p.Pro245Thr
ENST00000707115.1:c.733C>A	ENSP00000516744.1:p.Pro245Thr
ENST00000707116.1:c.733C>A	ENSP00000516745.1:p.Pro245Thr
ENST00000524013.2:c.775C>A	ENSP00000430235.2:p.Pro259Thr
ENST00000621592.8:c.778C>A MANE Select	ENSP00000478887.2:p.Pro260Thr
ENST00000651626.1:c.433C>A	ENSP00000499182.1:p.Pro145Thr
ENST00000652288.1:c.733C>A	ENSP00000499105.1:p.Pro245Thr
ENST00000259523.10:c.733C>A	ENSP00000259523.6:p.Pro245Thr
ENST00000377970.6:c.733C>A	ENSP00000367207.3:p.Pro245Thr
ENST00000524013.1:c.775C>A	ENSP00000430235.1:p.Pro259Thr
ENST00000613283.1:c.778C>A	ENSP00000479618.1:p.Pro260Thr
ENST00000621592.5:c.778C>A	ENSP00000478887.1:p.Pro260Thr
NM_002467.4:c.778C>A	NP_002458.2:p.Pro260Thr
NM_001354870.1:c.775C>A	NP_001341799.1:p.Pro259Thr
NM_002467.5:c.778C>A	NP_002458.2:p.Pro260Thr
NM_002467.6:c.778C>A MANE Select	NP_002458.2:p.Pro260Thr