Canonical Allele Identifier: CA10698645
Gene: MDM4 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs1380576

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.204519150G>C , CM000663.2:g.204519150G>C GRCh38
NC_000001.10:g.204488278G>C , CM000663.1:g.204488278G>C GRCh37
NC_000001.9:g.202754901G>C NCBI36
NG_029367.1:g.7772G>C

Transcript Alleles

HGVS Amino-acid change
NM_001204171.1:c.-36+2641G>C VV NP_001191100.1:p.=
NM_001204172.1:c.-36+2641G>C VV NP_001191101.1:p.=
NM_001278516.1:c.-36+2641G>C VV NP_001265445.1:p.=
NM_001278517.1:c.-36+2641G>C VV NP_001265446.1:p.=
NM_001278518.1:c.-36+2641G>C VV NP_001265447.1:p.=
NM_001278519.1:c.-36+2641G>C VV NP_001265448.1:p.=
NM_002393.4:c.-36+2641G>C VV NP_002384.2:p.=
XM_006711328.1:c.-36+2641G>C XP_006711391.1:p.=
XM_011509565.1:c.-36+2641G>C XP_011507867.1:p.=
XM_011509566.1:c.-36+2641G>C XP_011507868.1:p.=
XM_024447114.1:c.-36+2531G>C XP_024302882.1:p.=
XM_024447115.1:c.-36+655G>C XP_024302883.1:p.=
XR_001737183.1:n.117+2641G>C
ENST00000367182.7:c.-36+2641G>C ENSP00000356150.3:p.=
ENST00000367183.7:c.-36+2641G>C ENSP00000356151.3:p.=
ENST00000391947.6:c.-36+2641G>C ENSP00000375811.2:p.=
ENST00000454264.6:c.-36+2641G>C ENSP00000396840.2:p.=
ENST00000463049.5:n.104+2641G>C
ENST00000470797.5:n.127+2641G>C
ENST00000470908.5:n.59+2641G>C
ENST00000471783.1:n.38+2641G>C
ENST00000612738.4:c.-36+2641G>C ENSP00000478080.1:p.=
ENST00000614459.4:c.-36+2641G>C ENSP00000482388.1:p.=
ENST00000616250.4:c.-36+2641G>C ENSP00000478581.1:p.=
ENST00000621032.4:c.-36+2641G>C ENSP00000482479.1:p.=