Canonical Allele Identifier: CA2573332804

Gene: MYC

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.127738435_127738436delinsGT , CM000670.2:g.127738435_127738436delinsGT	GRCh38
NC_000008.10:g.128750681_128750682delinsGT , CM000670.1:g.128750681_128750682delinsGT	GRCh37
NC_000008.9:g.128819863_128819864delinsGT	NCBI36
NG_007161.1:g.7366_7367delinsGT
NG_007161.2:g.8002_8003delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000707113.1:c.173_174delinsGT	ENSP00000516742.1:p.Thr58Ser
ENST00000707114.1:c.173_174delinsGT	ENSP00000516743.1:p.Thr58Ser
ENST00000707115.1:c.173_174delinsGT	ENSP00000516744.1:p.Thr58Ser
ENST00000707116.1:c.173_174delinsGT	ENSP00000516745.1:p.Thr58Ser
ENST00000517291.2:c.215_216delinsGT	ENSP00000429441.2:p.Thr72Ser
ENST00000524013.2:c.215_216delinsGT	ENSP00000430235.2:p.Thr72Ser
ENST00000621592.8:c.218_219delinsGT MANE Select	ENSP00000478887.2:p.Thr73Ser
ENST00000651626.1:c.-128_-127delinsGT	ENSP00000499182.1:n.-128_-127delinsGT
ENST00000652288.1:c.173_174delinsGT	ENSP00000499105.1:p.Thr58Ser
ENST00000259523.10:c.173_174delinsGT	ENSP00000259523.6:p.Thr58Ser
ENST00000377970.6:c.173_174delinsGT	ENSP00000367207.3:p.Thr58Ser
ENST00000517291.1:c.215_216delinsGT	ENSP00000429441.1:p.Thr72Ser
ENST00000520751.1:c.139_140delinsGT	ENSP00000430226.1:p.Pro47Val
ENST00000524013.1:c.215_216delinsGT	ENSP00000430235.1:p.Thr72Ser
ENST00000613283.1:c.218_219delinsGT	ENSP00000479618.1:p.Thr73Ser
ENST00000621592.5:c.218_219delinsGT	ENSP00000478887.1:p.Thr73Ser
NM_002467.4:c.218_219delinsGT	NP_002458.2:p.Thr73Ser
NM_001354870.1:c.215_216delinsGT	NP_001341799.1:p.Thr72Ser
NM_002467.5:c.218_219delinsGT	NP_002458.2:p.Thr73Ser
NM_002467.6:c.218_219delinsGT MANE Select	NP_002458.2:p.Thr73Ser