Canonical Allele Identifier: CA1140014528

Gene: MDM4

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204549714C= , CM000663.2:g.204549714C=	GRCh38
NC_000001.10:g.204518842C= , CM000663.1:g.204518842C=	GRCh37
NC_000001.9:g.202785465C=	NCBI36
NG_029367.1:g.38336C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367182.8:c.*32C= MANE Select	ENSP00000356150.3:n.*32C=
ENST00000367182.7:c.*32C=	ENSP00000356150.3:n.*32C=
ENST00000367183.7:c.*32C=	ENSP00000356151.3:n.*32C=
ENST00000391947.6:c.*1014C=	ENSP00000375811.2:n.*1014C=
ENST00000454264.6:c.*32C=	ENSP00000396840.2:n.*32C=
ENST00000463049.5:n.1615C=
ENST00000612738.4:c.*32C=	ENSP00000478080.1:n.*32C=
ENST00000614459.4:c.*32C=	ENSP00000482388.1:n.*32C=
ENST00000616250.4:c.*675C=	ENSP00000478581.1:n.*675C=
ENST00000621032.4:c.*1014C=	ENSP00000482479.1:n.*1014C=
NM_001204171.1:c.*32C=	NP_001191100.1:n.*32C=
NM_001204172.1:c.*32C=	NP_001191101.1:n.*32C=
NM_001278516.1:c.*1014C=	NP_001265445.1:n.*1014C=
NM_001278517.1:c.*32C=	NP_001265446.1:n.*32C=
NM_001278518.1:c.*675C=	NP_001265447.1:n.*675C=
NM_001278519.1:c.*32C=	NP_001265448.1:n.*32C=
NM_002393.4:c.*32C=	NP_002384.2:n.*32C=
XM_006711328.1:c.*32C=	XP_006711391.1:n.*32C=
XM_011509565.1:c.953+552C=	XP_011507867.1:n.953+552C=
XM_017001311.1:c.*32C=	XP_016856800.1:n.*32C=
XM_017001312.1:c.*32C=	XP_016856801.1:n.*32C=
XM_017001313.1:c.*32C=	XP_016856802.1:n.*32C=
XM_024447114.1:c.*32C=	XP_024302882.1:n.*32C=
XM_024447115.1:c.*32C=	XP_024302883.1:n.*32C=
XR_001737179.1:n.1641C=
XR_001737180.2:n.1626C=
XR_001737181.1:n.1602C=
XR_001737183.1:n.1628C=
XR_002956626.1:n.1587C=
NM_002393.5:c.*32C= MANE Select	NP_002384.2:n.*32C=
NM_001204171.2:c.*32C=	NP_001191100.1:n.*32C=
NM_001204172.2:c.*32C=	NP_001191101.1:n.*32C=
NM_001278516.2:c.*1014C=	NP_001265445.1:n.*1014C=
NM_001278517.2:c.*32C=	NP_001265446.1:n.*32C=
NM_001278518.2:c.*675C=	NP_001265447.1:n.*675C=
NM_001278519.2:c.*32C=	NP_001265448.1:n.*32C=