Canonical Allele Identifier: CA1751419307
Gene: EZH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807676G= , CM000669.2:g.148807676G= GRCh38
NC_000007.13:g.148504768G= , CM000669.1:g.148504768G= GRCh37
NC_000007.12:g.148135701G= NCBI36
NG_032043.1:g.81674C= , LRG_531:g.81674C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000682263.1:n.4126C=
ENST00000682317.1:c.*1288C= ENSP00000508286.1:n.*1288C=
ENST00000683292.1:c.*1122C= ENSP00000507503.1:n.*1122C=
ENST00000683293.1:n.3945C=
ENST00000683744.1:c.*1288C= ENSP00000506949.1:n.*1288C=
ENST00000684300.1:c.*1288C= ENSP00000508407.1:n.*1288C=
ENST00000684400.1:n.4213C=
ENST00000684436.1:n.2542C=
ENST00000684510.1:n.2604C=
ENST00000320356.7:c.2226C= MANE Select ENSP00000320147.2:p.Val742=
ENST00000320356.6:c.2226C= ENSP00000320147.2:p.Val742=
ENST00000350995.6:c.2094C= ENSP00000223193.2:p.Val698=
ENST00000460911.5:c.2211C= ENSP00000419711.1:p.Val737=
ENST00000476773.5:c.2058C= ENSP00000419050.1:p.Val686=
ENST00000478654.5:c.2058C= ENSP00000417062.1:p.Val686=
ENST00000483967.5:c.2184C= ENSP00000419856.1:p.Val728=
ENST00000492143.5:c.*2216C= ENSP00000417377.1:n.*2216C=
NM_001203247.1:c.2211C= NP_001190176.1:p.Val737=
NM_001203248.1:c.2184C= NP_001190177.1:p.Val728=
NM_001203249.1:c.2058C= NP_001190178.1:p.Val686=
NM_004456.4:c.2226C= , LRG_531t1:c.2226C= NP_004447.2:p.Val742=
NM_152998.2:c.2094C= NP_694543.1:p.Val698=
XM_005249962.3:c.2235C= XP_005250019.1:p.Val745=
XM_005249963.3:c.2208C= XP_005250020.1:p.Val736=
XM_005249964.3:c.2082C= XP_005250021.1:p.Val694=
XM_011515883.1:c.2250C= XP_011514185.1:p.Val750=
XM_011515884.1:c.2226C= XP_011514186.1:p.Val742=
XM_011515885.1:c.2223C= XP_011514187.1:p.Val741=
XM_011515886.1:c.2202C= XP_011514188.1:p.Val734=
XM_011515887.1:c.2199C= XP_011514189.1:p.Val733=
XM_011515888.1:c.2199C= XP_011514190.1:p.Val733=
XM_011515889.1:c.2160C= XP_011514191.1:p.Val720=
XM_011515890.1:c.2133C= XP_011514192.1:p.Val711=
XM_011515891.1:c.2127C= XP_011514193.1:p.Val709=
XM_011515892.1:c.2124C= XP_011514194.1:p.Val708=
XM_011515893.1:c.2118C= XP_011514195.1:p.Val706=
XM_011515894.1:c.2109C= XP_011514196.1:p.Val703=
XM_011515895.1:c.2106C= XP_011514197.1:p.Val702=
XM_011515896.1:c.1992C= XP_011514198.1:p.Val664=
XM_011515897.1:c.1899C= XP_011514199.1:p.Val633=
XM_011515898.1:c.1899C= XP_011514200.1:p.Val633=
XR_928101.1:n.515+2591G=
XR_928102.1:n.722+2591G=
XM_005249962.4:c.2235C= XP_005250019.1:p.Val745=
XM_005249963.4:c.2208C= XP_005250020.1:p.Val736=
XM_005249964.4:c.2082C= XP_005250021.1:p.Val694=
XM_011515883.2:c.2250C= XP_011514185.1:p.Val750=
XM_011515884.2:c.2226C= XP_011514186.1:p.Val742=
XM_011515885.2:c.2223C= XP_011514187.1:p.Val741=
XM_011515886.2:c.2202C= XP_011514188.1:p.Val734=
XM_011515887.3:c.2199C= XP_011514189.1:p.Val733=
XM_011515888.2:c.2199C= XP_011514190.1:p.Val733=
XM_011515889.2:c.2160C= XP_011514191.1:p.Val720=
XM_011515890.2:c.2133C= XP_011514192.1:p.Val711=
XM_011515891.3:c.2127C= XP_011514193.1:p.Val709=
XM_011515892.2:c.2124C= XP_011514194.1:p.Val708=
XM_011515893.2:c.2118C= XP_011514195.1:p.Val706=
XM_011515894.2:c.2109C= XP_011514196.1:p.Val703=
XM_011515895.2:c.2106C= XP_011514197.1:p.Val702=
XM_011515896.2:c.1992C= XP_011514198.1:p.Val664=
XM_011515897.2:c.1899C= XP_011514199.1:p.Val633=
XM_011515898.2:c.1899C= XP_011514200.1:p.Val633=
XM_017011817.2:c.2250C= XP_016867306.1:p.Val750=
XM_017011818.1:c.2187C= XP_016867307.1:p.Val729=
XM_017011819.1:c.2109C= XP_016867308.1:p.Val703=
XM_017011820.2:c.2082C= XP_016867309.1:p.Val694=
XM_017011821.1:c.1884C= XP_016867310.1:p.Val628=
XM_024446680.1:c.2112C= XP_024302448.1:p.Val704=
XR_001744581.1:n.4600C=
XR_002956413.1:n.5256C=
XR_002956414.1:n.5716C=
NM_001203247.2:c.2211C= NP_001190176.1:p.Val737=
NM_001203248.2:c.2184C= NP_001190177.1:p.Val728=
NM_001203249.2:c.2058C= NP_001190178.1:p.Val686=
NM_004456.5:c.2226C= MANE Select NP_004447.2:p.Val742=
NM_152998.3:c.2094C= NP_694543.1:p.Val698=