Canonical Allele Identifier: CA6678878

Gene: MDM2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.68839587A>G , CM000674.2:g.68839587A>G	GRCh38
NC_000012.11:g.69233367A>G , CM000674.1:g.69233367A>G	GRCh37
NC_000012.10:g.67519634A>G	NCBI36
NG_016708.1:g.36397A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000258149.11:c.1232A>G MANE Select	ENSP00000258149.6:p.Tyr411Cys
ENST00000258149.10:c.1232A>G	ENSP00000258149.6:p.Tyr411Cys
ENST00000348801.7:c.537A>G
ENST00000393416.7:c.1307A>G	ENSP00000377068.3:p.Tyr436Cys
ENST00000393417.8:c.*1088A>G	ENSP00000429021.3:n.*1088A>G
ENST00000478070.2:c.431A>G
ENST00000481186.6:c.795A>G
ENST00000539479.6:c.1214A>G	ENSP00000444430.2:p.Tyr405Cys
ENST00000544561.6:c.1106A>G	ENSP00000441841.2:p.Tyr369Cys
ENST00000545204.2:c.492A>G	ENSP00000444597.2:n.492A>G
ENST00000665020.1:c.1098A>G	ENSP00000499718.1:n.1098A>G
ENST00000666617.1:c.1125A>G	ENSP00000499763.1:n.1125A>G
ENST00000671567.1:c.1153A>G	ENSP00000499407.1:n.1153A>G
ENST00000258148.11:c.1067A>G	ENSP00000258148.7:p.Tyr356Cys
ENST00000258149.9:c.1232A>G	ENSP00000258149.6:p.Tyr411Cys
ENST00000299252.8:c.704A>G	ENSP00000299252.4:p.Tyr235Cys
ENST00000311420.13:c.*843A>G	ENSP00000310742.9:n.*843A>G
ENST00000348801.6:c.536A>G	ENSP00000335096.3:p.Tyr179Cys
ENST00000350057.9:c.1139A>G	ENSP00000266624.9:p.Tyr380Cys
ENST00000356290.8:c.704A>G	ENSP00000348637.4:p.Tyr235Cys
ENST00000360430.6:c.629A>G	ENSP00000353611.2:p.Tyr210Cys
ENST00000393410.5:c.470A>G	ENSP00000377062.1:p.Tyr157Cys
ENST00000393412.7:c.470A>G	ENSP00000377064.4:p.Tyr157Cys
ENST00000393413.7:c.395A>G	ENSP00000377065.3:p.Tyr132Cys
ENST00000393417.7:c.*1088A>G	ENSP00000429021.2:n.*1088A>G
ENST00000428863.6:c.506-36A>G	ENSP00000410694.3:n.506-36A>G
ENST00000462284.5:c.1139A>G	ENSP00000417281.2:p.Tyr380Cys
ENST00000478070.1:c.430A>G	ENSP00000430906.1:n.430A>G
ENST00000481186.5:c.794A>G	ENSP00000431110.1:n.794A>G
ENST00000496959.5:c.635A>G	ENSP00000429692.1:n.635A>G
ENST00000517852.5:c.157-26A>G	ENSP00000430257.1:n.157-26A>G
ENST00000536089.5:c.919A>G	ENSP00000444028.1:n.919A>G
ENST00000537182.5:c.749A>G	ENSP00000443450.1:n.749A>G
ENST00000540352.5:c.1053A>G	ENSP00000445030.1:n.1053A>G
ENST00000542502.5:c.865A>G	ENSP00000444566.1:n.865A>G
ENST00000544561.5:c.184-175A>G	ENSP00000441841.1:n.184-175A>G
ENST00000545204.1:c.136A>G	ENSP00000444597.1:p.Ile46Val
ENST00000546048.5:c.289-188A>G	ENSP00000445222.1:n.289-188A>G
NM_001145337.2:c.1073A>G	NP_001138809.1:p.Tyr358Cys
NM_001145339.2:c.1067A>G	NP_001138811.1:p.Tyr356Cys
NM_001145340.2:c.626A>G	NP_001138812.1:p.Tyr209Cys
NM_001278462.1:c.704A>G	NP_001265391.1:p.Tyr235Cys
NM_002392.5:c.1232A>G	NP_002383.2:p.Tyr411Cys
XM_005268872.3:c.1214A>G	XP_005268929.1:p.Tyr405Cys
XM_006719399.2:c.1031A>G	XP_006719462.1:p.Tyr344Cys
XM_006719400.2:c.911A>G	XP_006719463.1:p.Tyr304Cys
XM_005268872.5:c.1214A>G	XP_005268929.1:p.Tyr405Cys
XM_006719399.4:c.1031A>G	XP_006719462.1:p.Tyr344Cys
XM_006719400.4:c.911A>G	XP_006719463.1:p.Tyr304Cys
NM_001145337.3:c.1073A>G	NP_001138809.1:p.Tyr358Cys
NM_001145340.3:c.626A>G	NP_001138812.1:p.Tyr209Cys
NM_001278462.2:c.704A>G	NP_001265391.1:p.Tyr235Cys
NM_001367990.1:c.1214A>G	NP_001354919.1:p.Tyr405Cys
NM_002392.6:c.1232A>G MANE Select	NP_002383.2:p.Tyr411Cys