Canonical Allele Identifier: CA16602893

Gene: MYC

Linked Data

• ClinVar Variation Id: 376459
• ClinVar RCV Id: RCV000418915 ; RCV000427867 ; RCV000428982 ; RCV000436178 ; RCV000438593
• dbSNP Id: rs1057519918
• MyVariant Identifiers: chr8:g.128750636C>T (hg19) ; chr8:g.127738390C>T (hg38)
• PubMed: PMID:26619011

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738390C>T , CM000670.2:g.127738390C>T	GRCh38
NC_000008.10:g.128750636C>T , CM000670.1:g.128750636C>T	GRCh37
NC_000008.9:g.128819818C>T	NCBI36
NG_007161.1:g.7321C>T
NG_007161.2:g.7957C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.128C>T	ENSP00000516742.1:p.Pro43Leu
ENST00000707114.1:c.128C>T	ENSP00000516743.1:p.Pro43Leu
ENST00000707115.1:c.128C>T	ENSP00000516744.1:p.Pro43Leu
ENST00000707116.1:c.128C>T	ENSP00000516745.1:p.Pro43Leu
ENST00000517291.2:c.170C>T	ENSP00000429441.2:p.Pro57Leu
ENST00000524013.2:c.170C>T	ENSP00000430235.2:p.Pro57Leu
ENST00000621592.8:c.173C>T MANE Select	ENSP00000478887.2:p.Pro58Leu
ENST00000651626.1:c.-173C>T	ENSP00000499182.1:n.-173C>T
ENST00000652288.1:c.128C>T	ENSP00000499105.1:p.Pro43Leu
ENST00000259523.10:c.128C>T	ENSP00000259523.6:p.Pro43Leu
ENST00000377970.6:c.128C>T	ENSP00000367207.3:p.Pro43Leu
ENST00000517291.1:c.170C>T	ENSP00000429441.1:p.Pro57Leu
ENST00000520751.1:c.94C>T	ENSP00000430226.1:p.Arg32Trp
ENST00000524013.1:c.170C>T	ENSP00000430235.1:p.Pro57Leu
ENST00000613283.1:c.173C>T	ENSP00000479618.1:p.Pro58Leu
ENST00000621592.5:c.173C>T	ENSP00000478887.1:p.Pro58Leu
NM_002467.4:c.173C>T	NP_002458.2:p.Pro58Leu
NM_001354870.1:c.170C>T	NP_001341799.1:p.Pro57Leu
NM_002467.5:c.173C>T	NP_002458.2:p.Pro58Leu
NM_002467.6:c.173C>T MANE Select	NP_002458.2:p.Pro58Leu