Canonical Allele Identifier: CA2579248078
Gene: MYC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127738372_127738373insTCA , CM000670.2:g.127738372_127738373insTCA GRCh38
NC_000008.10:g.128750618_128750619insTCA , CM000670.1:g.128750618_128750619insTCA GRCh37
NC_000008.9:g.128819800_128819801insTCA NCBI36
NG_007161.1:g.7303_7304insTCA
NG_007161.2:g.7939_7940insTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000707113.1:c.110_111insTCA ENSP00000516742.1:p.Gln36_Gln37insHis
ENST00000707114.1:c.110_111insTCA ENSP00000516743.1:p.Gln36_Gln37insHis
ENST00000707115.1:c.110_111insTCA ENSP00000516744.1:p.Gln36_Gln37insHis
ENST00000707116.1:c.110_111insTCA ENSP00000516745.1:p.Gln36_Gln37insHis
ENST00000517291.2:c.152_153insTCA ENSP00000429441.2:p.Gln50_Gln51insHis
ENST00000524013.2:c.152_153insTCA ENSP00000430235.2:p.Gln50_Gln51insHis
ENST00000621592.8:c.155_156insTCA MANE Select ENSP00000478887.2:p.Gln51_Gln52insHis
ENST00000651626.1:c.-191_-190insTCA ENSP00000499182.1:n.-191_-190insTCA
ENST00000652288.1:c.110_111insTCA ENSP00000499105.1:p.Gln36_Gln37insHis
ENST00000259523.10:c.110_111insTCA ENSP00000259523.6:p.Gln36_Gln37insHis
ENST00000377970.6:c.110_111insTCA ENSP00000367207.3:p.Gln36_Gln37insHis
ENST00000517291.1:c.152_153insTCA ENSP00000429441.1:p.Gln50_Gln51insHis
ENST00000520751.1:c.76_77insTCA ENSP00000430226.1:p.Ser25_Arg26insIle
ENST00000524013.1:c.152_153insTCA ENSP00000430235.1:p.Gln50_Gln51insHis
ENST00000613283.1:c.155_156insTCA ENSP00000479618.1:p.Gln51_Gln52insHis
ENST00000621592.5:c.155_156insTCA ENSP00000478887.1:p.Gln51_Gln52insHis
NM_002467.4:c.155_156insTCA NP_002458.2:p.Gln51_Gln52insHis
NM_001354870.1:c.152_153insTCA NP_001341799.1:p.Gln50_Gln51insHis
NM_002467.5:c.155_156insTCA NP_002458.2:p.Gln51_Gln52insHis
NM_002467.6:c.155_156insTCA MANE Select NP_002458.2:p.Gln51_Gln52insHis