Canonical Allele Identifier: CA1751422392
Gene: EZH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148810367T= , CM000669.2:g.148810367T= GRCh38
NC_000007.13:g.148507459T= , CM000669.1:g.148507459T= GRCh37
NC_000007.12:g.148138392T= NCBI36
NG_032043.1:g.78983A= , LRG_531:g.78983A=

Transcript Alleles

HGVS Amino-acid change
ENST00000682263.1:n.3895A=
ENST00000682317.1:c.*1057A= ENSP00000508286.1:n.*1057A=
ENST00000683292.1:c.*891A= ENSP00000507503.1:n.*891A=
ENST00000683293.1:n.3714A=
ENST00000683744.1:c.*1057A= ENSP00000506949.1:n.*1057A=
ENST00000684300.1:c.*1057A= ENSP00000508407.1:n.*1057A=
ENST00000684400.1:n.2886A=
ENST00000684436.1:n.2311A=
ENST00000684510.1:n.2373A=
ENST00000320356.7:c.1995A= MANE Select ENSP00000320147.2:p.Lys665=
ENST00000320356.6:c.1995A= ENSP00000320147.2:p.Lys665=
ENST00000350995.6:c.1863A= ENSP00000223193.2:p.Lys621=
ENST00000460911.5:c.1980A= ENSP00000419711.1:p.Lys660=
ENST00000469631.1:n.247A=
ENST00000476773.5:c.1827A= ENSP00000419050.1:p.Lys609=
ENST00000478654.5:c.1827A= ENSP00000417062.1:p.Lys609=
ENST00000483967.5:c.1953A= ENSP00000419856.1:p.Lys651=
ENST00000492143.5:c.*1985A= ENSP00000417377.1:n.*1985A=
NM_001203247.1:c.1980A= NP_001190176.1:p.Lys660=
NM_001203248.1:c.1953A= NP_001190177.1:p.Lys651=
NM_001203249.1:c.1827A= NP_001190178.1:p.Lys609=
NM_004456.4:c.1995A= , LRG_531t1:c.1995A= NP_004447.2:p.Lys665=
NM_152998.2:c.1863A= NP_694543.1:p.Lys621=
XM_005249962.3:c.2004A= XP_005250019.1:p.Lys668=
XM_005249963.3:c.1977A= XP_005250020.1:p.Lys659=
XM_005249964.3:c.1851A= XP_005250021.1:p.Lys617=
XM_011515883.1:c.2019A= XP_011514185.1:p.Lys673=
XM_011515884.1:c.1995A= XP_011514186.1:p.Lys665=
XM_011515885.1:c.1992A= XP_011514187.1:p.Lys664=
XM_011515886.1:c.1971A= XP_011514188.1:p.Lys657=
XM_011515887.1:c.1968A= XP_011514189.1:p.Lys656=
XM_011515888.1:c.1968A= XP_011514190.1:p.Lys656=
XM_011515889.1:c.1929A= XP_011514191.1:p.Lys643=
XM_011515890.1:c.1902A= XP_011514192.1:p.Lys634=
XM_011515891.1:c.1896A= XP_011514193.1:p.Lys632=
XM_011515892.1:c.1893A= XP_011514194.1:p.Lys631=
XM_011515893.1:c.1887A= XP_011514195.1:p.Lys629=
XM_011515894.1:c.1878A= XP_011514196.1:p.Lys626=
XM_011515895.1:c.1875A= XP_011514197.1:p.Lys625=
XM_011515896.1:c.1761A= XP_011514198.1:p.Lys587=
XM_011515897.1:c.1668A= XP_011514199.1:p.Lys556=
XM_011515898.1:c.1668A= XP_011514200.1:p.Lys556=
XR_928101.1:n.515+5282T=
XR_928102.1:n.722+5282T=
XM_005249962.4:c.2004A= XP_005250019.1:p.Lys668=
XM_005249963.4:c.1977A= XP_005250020.1:p.Lys659=
XM_005249964.4:c.1851A= XP_005250021.1:p.Lys617=
XM_011515883.2:c.2019A= XP_011514185.1:p.Lys673=
XM_011515884.2:c.1995A= XP_011514186.1:p.Lys665=
XM_011515885.2:c.1992A= XP_011514187.1:p.Lys664=
XM_011515886.2:c.1971A= XP_011514188.1:p.Lys657=
XM_011515887.3:c.1968A= XP_011514189.1:p.Lys656=
XM_011515888.2:c.1968A= XP_011514190.1:p.Lys656=
XM_011515889.2:c.1929A= XP_011514191.1:p.Lys643=
XM_011515890.2:c.1902A= XP_011514192.1:p.Lys634=
XM_011515891.3:c.1896A= XP_011514193.1:p.Lys632=
XM_011515892.2:c.1893A= XP_011514194.1:p.Lys631=
XM_011515893.2:c.1887A= XP_011514195.1:p.Lys629=
XM_011515894.2:c.1878A= XP_011514196.1:p.Lys626=
XM_011515895.2:c.1875A= XP_011514197.1:p.Lys625=
XM_011515896.2:c.1761A= XP_011514198.1:p.Lys587=
XM_011515897.2:c.1668A= XP_011514199.1:p.Lys556=
XM_011515898.2:c.1668A= XP_011514200.1:p.Lys556=
XM_017011817.2:c.2019A= XP_016867306.1:p.Lys673=
XM_017011818.1:c.1956A= XP_016867307.1:p.Lys652=
XM_017011819.1:c.1878A= XP_016867308.1:p.Lys626=
XM_017011820.2:c.1851A= XP_016867309.1:p.Lys617=
XM_017011821.1:c.1653A= XP_016867310.1:p.Lys551=
XM_024446680.1:c.1881A= XP_024302448.1:p.Lys627=
XR_001744581.1:n.4369A=
XR_002956413.1:n.5025A=
XR_002956414.1:n.5485A=
NM_001203247.2:c.1980A= NP_001190176.1:p.Lys660=
NM_001203248.2:c.1953A= NP_001190177.1:p.Lys651=
NM_001203249.2:c.1827A= NP_001190178.1:p.Lys609=
NM_004456.5:c.1995A= MANE Select NP_004447.2:p.Lys665=
NM_152998.3:c.1863A= NP_694543.1:p.Lys621=