Canonical Allele Identifier: CA2482203711
Gene: MDM4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204519043_204519045delinsTCA , CM000663.2:g.204519043_204519045delinsTCA GRCh38
NC_000001.10:g.204488171_204488173delinsTCA , CM000663.1:g.204488171_204488173delinsTCA GRCh37
NC_000001.9:g.202754794_202754796delinsTCA NCBI36
NG_029367.1:g.7665_7667delinsTCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000367182.8:c.-36+2534_-36+2536delinsTCA MANE Select ENSP00000356150.3:n.-36+2534_-36+2536delinsTCA
ENST00000367182.7:c.-36+2534_-36+2536delinsTCA ENSP00000356150.3:n.-36+2534_-36+2536delinsTCA
ENST00000367183.7:c.-36+2534_-36+2536delinsTCA ENSP00000356151.3:n.-36+2534_-36+2536delinsTCA
ENST00000391947.6:c.-36+2534_-36+2536delinsTCA ENSP00000375811.2:n.-36+2534_-36+2536delinsTCA
ENST00000454264.6:c.-36+2534_-36+2536delinsTCA ENSP00000396840.2:n.-36+2534_-36+2536delinsTCA
ENST00000463049.5:n.104+2534_104+2536delinsTCA
ENST00000470797.5:n.127+2534_127+2536delinsTCA
ENST00000470908.5:n.59+2534_59+2536delinsTCA
ENST00000471783.1:n.38+2534_38+2536delinsTCA
ENST00000612738.4:c.-36+2534_-36+2536delinsTCA ENSP00000478080.1:n.-36+2534_-36+2536delinsTCA
ENST00000614459.4:c.-36+2534_-36+2536delinsTCA ENSP00000482388.1:n.-36+2534_-36+2536delinsTCA
ENST00000616250.4:c.-36+2534_-36+2536delinsTCA ENSP00000478581.1:n.-36+2534_-36+2536delinsTCA
ENST00000621032.4:c.-36+2534_-36+2536delinsTCA ENSP00000482479.1:n.-36+2534_-36+2536delinsTCA
NM_001204171.1:c.-36+2534_-36+2536delinsTCA NP_001191100.1:n.-36+2534_-36+2536delinsTCA
NM_001204172.1:c.-36+2534_-36+2536delinsTCA NP_001191101.1:n.-36+2534_-36+2536delinsTCA
NM_001278516.1:c.-36+2534_-36+2536delinsTCA NP_001265445.1:n.-36+2534_-36+2536delinsTCA
NM_001278517.1:c.-36+2534_-36+2536delinsTCA NP_001265446.1:n.-36+2534_-36+2536delinsTCA
NM_001278518.1:c.-36+2534_-36+2536delinsTCA NP_001265447.1:n.-36+2534_-36+2536delinsTCA
NM_001278519.1:c.-36+2534_-36+2536delinsTCA NP_001265448.1:n.-36+2534_-36+2536delinsTCA
NM_002393.4:c.-36+2534_-36+2536delinsTCA NP_002384.2:n.-36+2534_-36+2536delinsTCA
XM_006711328.1:c.-36+2534_-36+2536delinsTCA XP_006711391.1:n.-36+2534_-36+2536delinsTCA
XM_011509565.1:c.-36+2534_-36+2536delinsTCA XP_011507867.1:n.-36+2534_-36+2536delinsTCA
XM_011509566.1:c.-36+2534_-36+2536delinsTCA XP_011507868.1:n.-36+2534_-36+2536delinsTCA
XM_024447114.1:c.-36+2424_-36+2426delinsTCA XP_024302882.1:n.-36+2424_-36+2426delinsTCA
XM_024447115.1:c.-36+548_-36+550delinsTCA XP_024302883.1:n.-36+548_-36+550delinsTCA
XR_001737183.1:n.117+2534_117+2536delinsTCA
NM_002393.5:c.-36+2534_-36+2536delinsTCA MANE Select NP_002384.2:n.-36+2534_-36+2536delinsTCA
NM_001204171.2:c.-36+2534_-36+2536delinsTCA NP_001191100.1:n.-36+2534_-36+2536delinsTCA
NM_001204172.2:c.-36+2534_-36+2536delinsTCA NP_001191101.1:n.-36+2534_-36+2536delinsTCA
NM_001278516.2:c.-36+2534_-36+2536delinsTCA NP_001265445.1:n.-36+2534_-36+2536delinsTCA
NM_001278517.2:c.-36+2534_-36+2536delinsTCA NP_001265446.1:n.-36+2534_-36+2536delinsTCA
NM_001278518.2:c.-36+2534_-36+2536delinsTCA NP_001265447.1:n.-36+2534_-36+2536delinsTCA
NM_001278519.2:c.-36+2534_-36+2536delinsTCA NP_001265448.1:n.-36+2534_-36+2536delinsTCA