Canonical Allele Identifier: CA585082713

Gene: MYC

Linked Data

• dbSNP Id: rs1220233528
• gnomAD v2: 8-128750459-CAA-C
• gnomAD v3: 8-127738213-CAA-C
• gnomAD v4: 8-127738213-CAA-C
• MyVariant Identifiers: chr8:g.128750460_128750461del (hg19) ; chr8:g.127738214_127738215del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738214_127738215del , CM000670.2:g.127738214_127738215del	GRCh38
NC_000008.10:g.128750460_128750461del , CM000670.1:g.128750460_128750461del	GRCh37
NC_000008.9:g.128819642_128819643del	NCBI36
NG_007161.1:g.7145_7146del
NG_007161.2:g.7781_7782del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.-15-34_-15-33del	ENSP00000516742.1:n.-15-34_-15-33del
ENST00000707114.1:c.-15-34_-15-33del	ENSP00000516743.1:n.-15-34_-15-33del
ENST00000707115.1:c.-49_-48del	ENSP00000516744.1:n.-49_-48del
ENST00000707116.1:c.-15-34_-15-33del	ENSP00000516745.1:n.-15-34_-15-33del
ENST00000517291.2:c.31-37_31-36del	ENSP00000429441.2:n.31-37_31-36del
ENST00000524013.2:c.31-37_31-36del	ENSP00000430235.2:n.31-37_31-36del
ENST00000621592.8:c.31-34_31-33del MANE Select	ENSP00000478887.2:n.31-34_31-33del
ENST00000651626.1:c.-283-66_-283-65del	ENSP00000499182.1:n.-283-66_-283-65del
ENST00000652288.1:c.-15-34_-15-33del	ENSP00000499105.1:n.-15-34_-15-33del
ENST00000259523.10:c.-15-34_-15-33del	ENSP00000259523.6:n.-15-34_-15-33del
ENST00000377970.6:c.-15-34_-15-33del	ENSP00000367207.3:n.-15-34_-15-33del
ENST00000517291.1:c.31-37_31-36del	ENSP00000429441.1:n.31-37_31-36del
ENST00000520751.1:c.-5-78_-5-77del	ENSP00000430226.1:n.-5-78_-5-77del
ENST00000524013.1:c.31-37_31-36del	ENSP00000430235.1:n.31-37_31-36del
ENST00000613283.1:c.31-34_31-33del	ENSP00000479618.1:n.31-34_31-33del
ENST00000621592.5:c.31-34_31-33del	ENSP00000478887.1:n.31-34_31-33del
NM_002467.4:c.31-34_31-33del	NP_002458.2:n.31-34_31-33del
NM_001354870.1:c.31-37_31-36del	NP_001341799.1:n.31-37_31-36del
NM_002467.5:c.31-34_31-33del	NP_002458.2:n.31-34_31-33del
NM_002467.6:c.31-34_31-33del MANE Select	NP_002458.2:n.31-34_31-33del