Canonical Allele Identifier: CA2688552146

Gene: MYC

Linked Data

• gnomAD v4: 8-127738190-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738190T>C , CM000670.2:g.127738190T>C	GRCh38
NC_000008.10:g.128750436T>C , CM000670.1:g.128750436T>C	GRCh37
NC_000008.9:g.128819618T>C	NCBI36
NG_007161.1:g.7121T>C
NG_007161.2:g.7757T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000707113.1:c.-15-58T>C	ENSP00000516742.1:n.-15-58T>C
ENST00000707114.1:c.-15-58T>C	ENSP00000516743.1:n.-15-58T>C
ENST00000707115.1:c.-73T>C	ENSP00000516744.1:n.-73T>C
ENST00000707116.1:c.-15-58T>C	ENSP00000516745.1:n.-15-58T>C
ENST00000517291.2:c.31-61T>C	ENSP00000429441.2:n.31-61T>C
ENST00000524013.2:c.31-61T>C	ENSP00000430235.2:n.31-61T>C
ENST00000621592.8:c.31-58T>C MANE Select	ENSP00000478887.2:n.31-58T>C
ENST00000651626.1:c.-283-90T>C	ENSP00000499182.1:n.-283-90T>C
ENST00000652288.1:c.-15-58T>C	ENSP00000499105.1:n.-15-58T>C
ENST00000259523.10:c.-15-58T>C	ENSP00000259523.6:n.-15-58T>C
ENST00000377970.6:c.-15-58T>C	ENSP00000367207.3:n.-15-58T>C
ENST00000517291.1:c.31-61T>C	ENSP00000429441.1:n.31-61T>C
ENST00000520751.1:c.-5-102T>C	ENSP00000430226.1:n.-5-102T>C
ENST00000524013.1:c.31-61T>C	ENSP00000430235.1:n.31-61T>C
ENST00000613283.1:c.31-58T>C	ENSP00000479618.1:n.31-58T>C
ENST00000621592.5:c.31-58T>C	ENSP00000478887.1:n.31-58T>C
NM_002467.4:c.31-58T>C	NP_002458.2:n.31-58T>C
NM_001354870.1:c.31-61T>C	NP_001341799.1:n.31-61T>C
NM_002467.5:c.31-58T>C	NP_002458.2:n.31-58T>C
NM_002467.6:c.31-58T>C MANE Select	NP_002458.2:n.31-58T>C