Canonical Allele Identifier: CA4875251

Gene: MYC

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738435C>G , CM000670.2:g.127738435C>G	GRCh38
NC_000008.10:g.128750681C>G , CM000670.1:g.128750681C>G	GRCh37
NC_000008.9:g.128819863C>G	NCBI36
NG_007161.1:g.7366C>G
NG_007161.2:g.8002C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.173C>G	ENSP00000516742.1:p.Thr58Ser
ENST00000707114.1:c.173C>G	ENSP00000516743.1:p.Thr58Ser
ENST00000707115.1:c.173C>G	ENSP00000516744.1:p.Thr58Ser
ENST00000707116.1:c.173C>G	ENSP00000516745.1:p.Thr58Ser
ENST00000517291.2:c.215C>G	ENSP00000429441.2:p.Thr72Ser
ENST00000524013.2:c.215C>G	ENSP00000430235.2:p.Thr72Ser
ENST00000621592.8:c.218C>G MANE Select	ENSP00000478887.2:p.Thr73Ser
ENST00000651626.1:c.-128C>G	ENSP00000499182.1:n.-128C>G
ENST00000652288.1:c.173C>G	ENSP00000499105.1:p.Thr58Ser
ENST00000259523.10:c.173C>G	ENSP00000259523.6:p.Thr58Ser
ENST00000377970.6:c.173C>G	ENSP00000367207.3:p.Thr58Ser
ENST00000517291.1:c.215C>G	ENSP00000429441.1:p.Thr72Ser
ENST00000520751.1:c.139C>G	ENSP00000430226.1:p.Pro47Ala
ENST00000524013.1:c.215C>G	ENSP00000430235.1:p.Thr72Ser
ENST00000613283.1:c.218C>G	ENSP00000479618.1:p.Thr73Ser
ENST00000621592.5:c.218C>G	ENSP00000478887.1:p.Thr73Ser
NM_002467.4:c.218C>G	NP_002458.2:p.Thr73Ser
NM_001354870.1:c.215C>G	NP_001341799.1:p.Thr72Ser
NM_002467.5:c.218C>G	NP_002458.2:p.Thr73Ser
NM_002467.6:c.218C>G MANE Select	NP_002458.2:p.Thr73Ser