Canonical Allele Identifier: CA2482203744

Gene: MDM4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204519105_204519106delinsAG , CM000663.2:g.204519105_204519106delinsAG	GRCh38
NC_000001.10:g.204488233_204488234delinsAG , CM000663.1:g.204488233_204488234delinsAG	GRCh37
NC_000001.9:g.202754856_202754857delinsAG	NCBI36
NG_029367.1:g.7727_7728delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367182.8:c.-36+2596_-36+2597delinsAG MANE Select	ENSP00000356150.3:n.-36+2596_-36+2597delinsAG
ENST00000367182.7:c.-36+2596_-36+2597delinsAG	ENSP00000356150.3:n.-36+2596_-36+2597delinsAG
ENST00000367183.7:c.-36+2596_-36+2597delinsAG	ENSP00000356151.3:n.-36+2596_-36+2597delinsAG
ENST00000391947.6:c.-36+2596_-36+2597delinsAG	ENSP00000375811.2:n.-36+2596_-36+2597delinsAG
ENST00000454264.6:c.-36+2596_-36+2597delinsAG	ENSP00000396840.2:n.-36+2596_-36+2597delinsAG
ENST00000463049.5:n.104+2596_104+2597delinsAG
ENST00000470797.5:n.127+2596_127+2597delinsAG
ENST00000470908.5:n.59+2596_59+2597delinsAG
ENST00000471783.1:n.38+2596_38+2597delinsAG
ENST00000612738.4:c.-36+2596_-36+2597delinsAG	ENSP00000478080.1:n.-36+2596_-36+2597delinsAG
ENST00000614459.4:c.-36+2596_-36+2597delinsAG	ENSP00000482388.1:n.-36+2596_-36+2597delinsAG
ENST00000616250.4:c.-36+2596_-36+2597delinsAG	ENSP00000478581.1:n.-36+2596_-36+2597delinsAG
ENST00000621032.4:c.-36+2596_-36+2597delinsAG	ENSP00000482479.1:n.-36+2596_-36+2597delinsAG
NM_001204171.1:c.-36+2596_-36+2597delinsAG	NP_001191100.1:n.-36+2596_-36+2597delinsAG
NM_001204172.1:c.-36+2596_-36+2597delinsAG	NP_001191101.1:n.-36+2596_-36+2597delinsAG
NM_001278516.1:c.-36+2596_-36+2597delinsAG	NP_001265445.1:n.-36+2596_-36+2597delinsAG
NM_001278517.1:c.-36+2596_-36+2597delinsAG	NP_001265446.1:n.-36+2596_-36+2597delinsAG
NM_001278518.1:c.-36+2596_-36+2597delinsAG	NP_001265447.1:n.-36+2596_-36+2597delinsAG
NM_001278519.1:c.-36+2596_-36+2597delinsAG	NP_001265448.1:n.-36+2596_-36+2597delinsAG
NM_002393.4:c.-36+2596_-36+2597delinsAG	NP_002384.2:n.-36+2596_-36+2597delinsAG
XM_006711328.1:c.-36+2596_-36+2597delinsAG	XP_006711391.1:n.-36+2596_-36+2597delinsAG
XM_011509565.1:c.-36+2596_-36+2597delinsAG	XP_011507867.1:n.-36+2596_-36+2597delinsAG
XM_011509566.1:c.-36+2596_-36+2597delinsAG	XP_011507868.1:n.-36+2596_-36+2597delinsAG
XM_024447114.1:c.-36+2486_-36+2487delinsAG	XP_024302882.1:n.-36+2486_-36+2487delinsAG
XM_024447115.1:c.-36+610_-36+611delinsAG	XP_024302883.1:n.-36+610_-36+611delinsAG
XR_001737183.1:n.117+2596_117+2597delinsAG
NM_002393.5:c.-36+2596_-36+2597delinsAG MANE Select	NP_002384.2:n.-36+2596_-36+2597delinsAG
NM_001204171.2:c.-36+2596_-36+2597delinsAG	NP_001191100.1:n.-36+2596_-36+2597delinsAG
NM_001204172.2:c.-36+2596_-36+2597delinsAG	NP_001191101.1:n.-36+2596_-36+2597delinsAG
NM_001278516.2:c.-36+2596_-36+2597delinsAG	NP_001265445.1:n.-36+2596_-36+2597delinsAG
NM_001278517.2:c.-36+2596_-36+2597delinsAG	NP_001265446.1:n.-36+2596_-36+2597delinsAG
NM_001278518.2:c.-36+2596_-36+2597delinsAG	NP_001265447.1:n.-36+2596_-36+2597delinsAG
NM_001278519.2:c.-36+2596_-36+2597delinsAG	NP_001265448.1:n.-36+2596_-36+2597delinsAG