Canonical Allele Identifier: CA2688552185

Gene: MYC

Linked Data

• gnomAD v4: 8-127738354-TCTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738356_127738358del , CM000670.2:g.127738356_127738358del	GRCh38
NC_000008.10:g.128750602_128750604del , CM000670.1:g.128750602_128750604del	GRCh37
NC_000008.9:g.128819784_128819786del	NCBI36
NG_007161.1:g.7287_7289del
NG_007161.2:g.7923_7925del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.94_96del	ENSP00000516742.1:p.Tyr32del
ENST00000707114.1:c.94_96del	ENSP00000516743.1:p.Tyr32del
ENST00000707115.1:c.94_96del	ENSP00000516744.1:p.Tyr32del
ENST00000707116.1:c.94_96del	ENSP00000516745.1:p.Tyr32del
ENST00000517291.2:c.136_138del	ENSP00000429441.2:p.Tyr46del
ENST00000524013.2:c.136_138del	ENSP00000430235.2:p.Tyr46del
ENST00000621592.8:c.139_141del MANE Select	ENSP00000478887.2:p.Tyr47del
ENST00000651626.1:c.-207_-205del	ENSP00000499182.1:n.-207_-205del
ENST00000652288.1:c.94_96del	ENSP00000499105.1:p.Tyr32del
ENST00000259523.10:c.94_96del	ENSP00000259523.6:p.Tyr32del
ENST00000377970.6:c.94_96del	ENSP00000367207.3:p.Tyr32del
ENST00000517291.1:c.136_138del	ENSP00000429441.1:p.Tyr46del
ENST00000520751.1:c.60_62del	ENSP00000430226.1:p.Thr21del
ENST00000524013.1:c.136_138del	ENSP00000430235.1:p.Tyr46del
ENST00000613283.1:c.139_141del	ENSP00000479618.1:p.Tyr47del
ENST00000621592.5:c.139_141del	ENSP00000478887.1:p.Tyr47del
NM_002467.4:c.139_141del	NP_002458.2:p.Tyr47del
NM_001354870.1:c.136_138del	NP_001341799.1:p.Tyr46del
NM_002467.5:c.139_141del	NP_002458.2:p.Tyr47del
NM_002467.6:c.139_141del MANE Select	NP_002458.2:p.Tyr47del