Canonical Allele Identifier: CA10698657
Gene: MDM4 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204539019G>A , CM000663.2:g.204539019G>A GRCh38
NC_000001.10:g.204508147G>A , CM000663.1:g.204508147G>A GRCh37
NC_000001.9:g.202774770G>A NCBI36
NG_029367.1:g.27641G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367182.8:c.511+711G>A MANE Select ENSP00000356150.3:n.511+711G>A
ENST00000367179.7:c.166+711G>A ENSP00000356147.3:n.166+711G>A
ENST00000367182.7:c.511+711G>A ENSP00000356150.3:n.511+711G>A
ENST00000367183.7:c.79-10247G>A ENSP00000356151.3:n.79-10247G>A
ENST00000391947.6:c.*20+711G>A ENSP00000375811.2:n.*20+711G>A
ENST00000454264.6:c.511+711G>A ENSP00000396840.2:n.511+711G>A
ENST00000462012.1:n.434+711G>A
ENST00000463049.5:n.621+711G>A
ENST00000470908.5:n.537+711G>A
ENST00000471783.1:n.326+711G>A
ENST00000507825.3:c.443+711G>A ENSP00000443816.2:n.443+711G>A
ENST00000612738.4:c.154-7778G>A ENSP00000478080.1:n.154-7778G>A
ENST00000614459.4:c.217+711G>A ENSP00000482388.1:n.217+711G>A
ENST00000616250.4:c.343+6773G>A ENSP00000478581.1:n.343+6773G>A
ENST00000621032.4:c.*20+711G>A ENSP00000482479.1:n.*20+711G>A
NM_001204171.1:c.511+711G>A NP_001191100.1:n.511+711G>A
NM_001204172.1:c.79-10247G>A NP_001191101.1:n.79-10247G>A
NM_001278516.1:c.*20+711G>A NP_001265445.1:n.*20+711G>A
NM_001278517.1:c.217+711G>A NP_001265446.1:n.217+711G>A
NM_001278518.1:c.343+6773G>A NP_001265447.1:n.343+6773G>A
NM_001278519.1:c.154-7778G>A NP_001265448.1:n.154-7778G>A
NM_002393.4:c.511+711G>A NP_002384.2:n.511+711G>A
XM_006711328.1:c.511+711G>A XP_006711391.1:n.511+711G>A
XM_011509565.1:c.511+711G>A XP_011507867.1:n.511+711G>A
XM_011509566.1:c.*20+711G>A XP_011507868.1:n.*20+711G>A
XM_011509568.1:c.*20+711G>A XP_011507870.1:n.*20+711G>A
XM_017001311.1:c.565+711G>A XP_016856800.1:n.565+711G>A
XM_017001312.1:c.565+711G>A XP_016856801.1:n.565+711G>A
XM_017001313.1:c.565+711G>A XP_016856802.1:n.565+711G>A
XM_024447114.1:c.511+711G>A XP_024302882.1:n.511+711G>A
XM_024447115.1:c.511+711G>A XP_024302883.1:n.511+711G>A
XR_001737179.1:n.647+711G>A
XR_001737180.2:n.647+711G>A
XR_001737181.1:n.608+711G>A
XR_001737182.1:n.608+711G>A
XR_001737183.1:n.634+711G>A
XR_002956626.1:n.608+711G>A
NM_002393.5:c.511+711G>A MANE Select NP_002384.2:n.511+711G>A
NM_001204171.2:c.511+711G>A NP_001191100.1:n.511+711G>A
NM_001204172.2:c.79-10247G>A NP_001191101.1:n.79-10247G>A
NM_001278516.2:c.*20+711G>A NP_001265445.1:n.*20+711G>A
NM_001278517.2:c.217+711G>A NP_001265446.1:n.217+711G>A
NM_001278518.2:c.343+6773G>A NP_001265447.1:n.343+6773G>A
NM_001278519.2:c.154-7778G>A NP_001265448.1:n.154-7778G>A
Search 100 bp 5'
Search 100 bp 3'