Canonical Allele Identifier: CA2482203795

Gene: MDM4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204519231_204519234delinsATTT , CM000663.2:g.204519231_204519234delinsATTT	GRCh38
NC_000001.10:g.204488359_204488362delinsATTT , CM000663.1:g.204488359_204488362delinsATTT	GRCh37
NC_000001.9:g.202754982_202754985delinsATTT	NCBI36
NG_029367.1:g.7853_7856delinsATTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367182.8:c.-36+2722_-36+2725delinsATTT MANE Select	ENSP00000356150.3:n.-36+2722_-36+2725delinsATTT
ENST00000367182.7:c.-36+2722_-36+2725delinsATTT	ENSP00000356150.3:n.-36+2722_-36+2725delinsATTT
ENST00000367183.7:c.-36+2722_-36+2725delinsATTT	ENSP00000356151.3:n.-36+2722_-36+2725delinsATTT
ENST00000391947.6:c.-36+2722_-36+2725delinsATTT	ENSP00000375811.2:n.-36+2722_-36+2725delinsATTT
ENST00000454264.6:c.-36+2722_-36+2725delinsATTT	ENSP00000396840.2:n.-36+2722_-36+2725delinsATTT
ENST00000463049.5:n.104+2722_104+2725delinsATTT
ENST00000470797.5:n.127+2722_127+2725delinsATTT
ENST00000470908.5:n.59+2722_59+2725delinsATTT
ENST00000471783.1:n.38+2722_38+2725delinsATTT
ENST00000612738.4:c.-36+2722_-36+2725delinsATTT	ENSP00000478080.1:n.-36+2722_-36+2725delinsATTT
ENST00000614459.4:c.-36+2722_-36+2725delinsATTT	ENSP00000482388.1:n.-36+2722_-36+2725delinsATTT
ENST00000616250.4:c.-36+2722_-36+2725delinsATTT	ENSP00000478581.1:n.-36+2722_-36+2725delinsATTT
ENST00000621032.4:c.-36+2722_-36+2725delinsATTT	ENSP00000482479.1:n.-36+2722_-36+2725delinsATTT
NM_001204171.1:c.-36+2722_-36+2725delinsATTT	NP_001191100.1:n.-36+2722_-36+2725delinsATTT
NM_001204172.1:c.-36+2722_-36+2725delinsATTT	NP_001191101.1:n.-36+2722_-36+2725delinsATTT
NM_001278516.1:c.-36+2722_-36+2725delinsATTT	NP_001265445.1:n.-36+2722_-36+2725delinsATTT
NM_001278517.1:c.-36+2722_-36+2725delinsATTT	NP_001265446.1:n.-36+2722_-36+2725delinsATTT
NM_001278518.1:c.-36+2722_-36+2725delinsATTT	NP_001265447.1:n.-36+2722_-36+2725delinsATTT
NM_001278519.1:c.-36+2722_-36+2725delinsATTT	NP_001265448.1:n.-36+2722_-36+2725delinsATTT
NM_002393.4:c.-36+2722_-36+2725delinsATTT	NP_002384.2:n.-36+2722_-36+2725delinsATTT
XM_006711328.1:c.-36+2722_-36+2725delinsATTT	XP_006711391.1:n.-36+2722_-36+2725delinsATTT
XM_011509565.1:c.-36+2722_-36+2725delinsATTT	XP_011507867.1:n.-36+2722_-36+2725delinsATTT
XM_011509566.1:c.-36+2722_-36+2725delinsATTT	XP_011507868.1:n.-36+2722_-36+2725delinsATTT
XM_024447114.1:c.-36+2612_-36+2615delinsATTT	XP_024302882.1:n.-36+2612_-36+2615delinsATTT
XM_024447115.1:c.-36+736_-36+739delinsATTT	XP_024302883.1:n.-36+736_-36+739delinsATTT
XR_001737183.1:n.117+2722_117+2725delinsATTT
NM_002393.5:c.-36+2722_-36+2725delinsATTT MANE Select	NP_002384.2:n.-36+2722_-36+2725delinsATTT
NM_001204171.2:c.-36+2722_-36+2725delinsATTT	NP_001191100.1:n.-36+2722_-36+2725delinsATTT
NM_001204172.2:c.-36+2722_-36+2725delinsATTT	NP_001191101.1:n.-36+2722_-36+2725delinsATTT
NM_001278516.2:c.-36+2722_-36+2725delinsATTT	NP_001265445.1:n.-36+2722_-36+2725delinsATTT
NM_001278517.2:c.-36+2722_-36+2725delinsATTT	NP_001265446.1:n.-36+2722_-36+2725delinsATTT
NM_001278518.2:c.-36+2722_-36+2725delinsATTT	NP_001265447.1:n.-36+2722_-36+2725delinsATTT
NM_001278519.2:c.-36+2722_-36+2725delinsATTT	NP_001265448.1:n.-36+2722_-36+2725delinsATTT