Canonical Allele Identifier: CA122526

Gene: MYC

Linked Data

• ClinVar Variation Id: 12577
• ClinVar RCV Id: RCV000013405 ; RCV003159073
• dbSNP Id: rs121918685
• COSMIC: COSM5656308 ; COSM5656309
• MyVariant Identifiers: chr8:g.128750683C>G (hg19) ; chr8:g.127738437C>G (hg38)
• PubMed: PMID:8220424

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738437C>G , CM000670.2:g.127738437C>G	GRCh38
NC_000008.10:g.128750683C>G , CM000670.1:g.128750683C>G	GRCh37
NC_000008.9:g.128819865C>G	NCBI36
NG_007161.1:g.7368C>G
NG_007161.2:g.8004C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000707113.1:c.175C>G	ENSP00000516742.1:p.Pro59Ala
ENST00000707114.1:c.175C>G	ENSP00000516743.1:p.Pro59Ala
ENST00000707115.1:c.175C>G	ENSP00000516744.1:p.Pro59Ala
ENST00000707116.1:c.175C>G	ENSP00000516745.1:p.Pro59Ala
ENST00000517291.2:c.217C>G	ENSP00000429441.2:p.Pro73Ala
ENST00000524013.2:c.217C>G	ENSP00000430235.2:p.Pro73Ala
ENST00000621592.8:c.220C>G MANE Select	ENSP00000478887.2:p.Pro74Ala
ENST00000651626.1:c.-126C>G	ENSP00000499182.1:n.-126C>G
ENST00000652288.1:c.175C>G	ENSP00000499105.1:p.Pro59Ala
ENST00000259523.10:c.175C>G	ENSP00000259523.6:p.Pro59Ala
ENST00000377970.6:c.175C>G	ENSP00000367207.3:p.Pro59Ala
ENST00000517291.1:c.217C>G	ENSP00000429441.1:p.Pro73Ala
ENST00000520751.1:c.141C>G	ENSP00000430226.1:p.Pro47=
ENST00000524013.1:c.217C>G	ENSP00000430235.1:p.Pro73Ala
ENST00000613283.1:c.220C>G	ENSP00000479618.1:p.Pro74Ala
ENST00000621592.5:c.220C>G	ENSP00000478887.1:p.Pro74Ala
NM_002467.4:c.220C>G	NP_002458.2:p.Pro74Ala
NM_001354870.1:c.217C>G	NP_001341799.1:p.Pro73Ala
NM_002467.5:c.220C>G	NP_002458.2:p.Pro74Ala
NM_002467.6:c.220C>G MANE Select	NP_002458.2:p.Pro74Ala