Canonical Allele Identifier: CA372279495

Gene: MYC

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738384A>C , CM000670.2:g.127738384A>C	GRCh38
NC_000008.10:g.128750630A>C , CM000670.1:g.128750630A>C	GRCh37
NC_000008.9:g.128819812A>C	NCBI36
NG_007161.1:g.7315A>C
NG_007161.2:g.7951A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.122A>C	ENSP00000516742.1:p.Gln41Pro
ENST00000707114.1:c.122A>C	ENSP00000516743.1:p.Gln41Pro
ENST00000707115.1:c.122A>C	ENSP00000516744.1:p.Gln41Pro
ENST00000707116.1:c.122A>C	ENSP00000516745.1:p.Gln41Pro
ENST00000517291.2:c.164A>C	ENSP00000429441.2:p.Gln55Pro
ENST00000524013.2:c.164A>C	ENSP00000430235.2:p.Gln55Pro
ENST00000621592.8:c.167A>C MANE Select	ENSP00000478887.2:p.Gln56Pro
ENST00000651626.1:c.-179A>C	ENSP00000499182.1:n.-179A>C
ENST00000652288.1:c.122A>C	ENSP00000499105.1:p.Gln41Pro
ENST00000259523.10:c.122A>C	ENSP00000259523.6:p.Gln41Pro
ENST00000377970.6:c.122A>C	ENSP00000367207.3:p.Gln41Pro
ENST00000517291.1:c.164A>C	ENSP00000429441.1:p.Gln55Pro
ENST00000520751.1:c.88A>C	ENSP00000430226.1:p.Ser30Arg
ENST00000524013.1:c.164A>C	ENSP00000430235.1:p.Gln55Pro
ENST00000613283.1:c.167A>C	ENSP00000479618.1:p.Gln56Pro
ENST00000621592.5:c.167A>C	ENSP00000478887.1:p.Gln56Pro
NM_002467.4:c.167A>C	NP_002458.2:p.Gln56Pro
NM_001354870.1:c.164A>C	NP_001341799.1:p.Gln55Pro
NM_002467.5:c.167A>C	NP_002458.2:p.Gln56Pro
NM_002467.6:c.167A>C MANE Select	NP_002458.2:p.Gln56Pro