Canonical Allele Identifier: CA2650053361

Gene: MDM4

Linked Data

• gnomAD v4: 1-204556351-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.204556351T>C , CM000663.2:g.204556351T>C	GRCh38
NC_000001.10:g.204525479T>C , CM000663.1:g.204525479T>C	GRCh37
NC_000001.9:g.202792102T>C	NCBI36
NG_029367.1:g.44973T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367182.8:c.*6669T>C MANE Select	ENSP00000356150.3:n.*6669T>C
ENST00000367182.7:c.*6669T>C	ENSP00000356150.3:n.*6669T>C
ENST00000367183.7:c.*6669T>C	ENSP00000356151.3:n.*6669T>C
ENST00000391947.6:c.*7651T>C	ENSP00000375811.2:n.*7651T>C
ENST00000454264.6:c.*6669T>C	ENSP00000396840.2:n.*6669T>C
ENST00000612738.4:c.*6669T>C	ENSP00000478080.1:n.*6669T>C
ENST00000614459.4:c.*6669T>C	ENSP00000482388.1:n.*6669T>C
ENST00000616250.4:c.*7312T>C	ENSP00000478581.1:n.*7312T>C
NM_001204171.1:c.*6669T>C	NP_001191100.1:n.*6669T>C
NM_001204172.1:c.*6669T>C	NP_001191101.1:n.*6669T>C
NM_001278516.1:c.*7651T>C	NP_001265445.1:n.*7651T>C
NM_001278517.1:c.*6669T>C	NP_001265446.1:n.*6669T>C
NM_001278518.1:c.*7312T>C	NP_001265447.1:n.*7312T>C
NM_001278519.1:c.*6669T>C	NP_001265448.1:n.*6669T>C
NM_002393.4:c.*6669T>C	NP_002384.2:n.*6669T>C
XM_011509565.1:c.954-2290T>C	XP_011507867.1:n.954-2290T>C
NM_002393.5:c.*6669T>C MANE Select	NP_002384.2:n.*6669T>C
NM_001204171.2:c.*6669T>C	NP_001191100.1:n.*6669T>C
NM_001204172.2:c.*6669T>C	NP_001191101.1:n.*6669T>C
NM_001278516.2:c.*7651T>C	NP_001265445.1:n.*7651T>C
NM_001278517.2:c.*6669T>C	NP_001265446.1:n.*6669T>C
NM_001278518.2:c.*7312T>C	NP_001265447.1:n.*7312T>C
NM_001278519.2:c.*6669T>C	NP_001265448.1:n.*6669T>C