Canonical Allele Identifier: CA2838266500

Gene: EZH2

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.148826367G>A , CM000669.2:g.148826367G>A	GRCh38
NC_000007.13:g.148523459G>A , CM000669.1:g.148523459G>A	GRCh37
NC_000007.12:g.148154392G>A	NCBI36
NG_032043.1:g.62983C>T , LRG_531:g.62983C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682263.1:n.1040+102C>T
ENST00000682317.1:c.775+102C>T	ENSP00000508286.1:n.775+102C>T
ENST00000682401.1:n.907+102C>T
ENST00000683292.1:c.565+102C>T	ENSP00000507503.1:n.565+102C>T
ENST00000683744.1:c.892+102C>T	ENSP00000506949.1:n.892+102C>T
ENST00000684300.1:c.775+102C>T	ENSP00000508407.1:n.775+102C>T
ENST00000320356.7:c.907+87C>T MANE Select	ENSP00000320147.2:n.907+87C>T
ENST00000320356.6:c.907+87C>T	ENSP00000320147.2:n.907+87C>T
ENST00000350995.6:c.775+102C>T	ENSP00000223193.2:n.775+102C>T
ENST00000460911.5:c.892+102C>T	ENSP00000419711.1:n.892+102C>T
ENST00000476773.5:c.865+102C>T	ENSP00000419050.1:n.865+102C>T
ENST00000478654.5:c.865+102C>T	ENSP00000417062.1:n.865+102C>T
ENST00000483012.1:c.*636+102C>T	ENSP00000417704.1:n.*636+102C>T
ENST00000483967.5:c.865+102C>T	ENSP00000419856.1:n.865+102C>T
ENST00000492143.5:c.892+102C>T	ENSP00000417377.1:n.892+102C>T
ENST00000498186.5:n.1023+102C>T
NM_001203247.1:c.892+102C>T	NP_001190176.1:n.892+102C>T
NM_001203248.1:c.865+102C>T	NP_001190177.1:n.865+102C>T
NM_001203249.1:c.865+102C>T	NP_001190178.1:n.865+102C>T
NM_004456.4:c.907+87C>T , LRG_531t1:c.907+87C>T	NP_004447.2:n.907+87C>T
NM_152998.2:c.775+102C>T	NP_694543.1:n.775+102C>T
XM_005249962.3:c.916+102C>T	XP_005250019.1:n.916+102C>T
XM_005249963.3:c.889+102C>T	XP_005250020.1:n.889+102C>T
XM_005249964.3:c.889+102C>T	XP_005250021.1:n.889+102C>T
XM_011515883.1:c.931+87C>T	XP_011514185.1:n.931+87C>T
XM_011515884.1:c.907+87C>T	XP_011514186.1:n.907+87C>T
XM_011515885.1:c.904+87C>T	XP_011514187.1:n.904+87C>T
XM_011515886.1:c.883+87C>T	XP_011514188.1:n.883+87C>T
XM_011515887.1:c.880+87C>T	XP_011514189.1:n.880+87C>T
XM_011515888.1:c.880+87C>T	XP_011514190.1:n.880+87C>T
XM_011515889.1:c.841+87C>T	XP_011514191.1:n.841+87C>T
XM_011515890.1:c.814+87C>T	XP_011514192.1:n.814+87C>T
XM_011515891.1:c.808+87C>T	XP_011514193.1:n.808+87C>T
XM_011515892.1:c.931+87C>T	XP_011514194.1:n.931+87C>T
XM_011515893.1:c.799+102C>T	XP_011514195.1:n.799+102C>T
XM_011515894.1:c.790+87C>T	XP_011514196.1:n.790+87C>T
XM_011515895.1:c.787+87C>T	XP_011514197.1:n.787+87C>T
XM_011515896.1:c.799+102C>T	XP_011514198.1:n.799+102C>T
XM_011515897.1:c.580+87C>T	XP_011514199.1:n.580+87C>T
XM_011515898.1:c.580+87C>T	XP_011514200.1:n.580+87C>T
XM_011515899.1:c.931+87C>T	XP_011514201.1:n.931+87C>T
XM_011515900.1:c.931+87C>T	XP_011514202.1:n.931+87C>T
XM_011515901.1:c.931+87C>T	XP_011514203.1:n.931+87C>T
XM_011515902.1:c.931+87C>T	XP_011514204.1:n.931+87C>T
XM_005249962.4:c.916+102C>T	XP_005250019.1:n.916+102C>T
XM_005249963.4:c.889+102C>T	XP_005250020.1:n.889+102C>T
XM_005249964.4:c.889+102C>T	XP_005250021.1:n.889+102C>T
XM_011515883.2:c.931+87C>T	XP_011514185.1:n.931+87C>T
XM_011515884.2:c.907+87C>T	XP_011514186.1:n.907+87C>T
XM_011515885.2:c.904+87C>T	XP_011514187.1:n.904+87C>T
XM_011515886.2:c.883+87C>T	XP_011514188.1:n.883+87C>T
XM_011515887.3:c.880+87C>T	XP_011514189.1:n.880+87C>T
XM_011515888.2:c.880+87C>T	XP_011514190.1:n.880+87C>T
XM_011515889.2:c.841+87C>T	XP_011514191.1:n.841+87C>T
XM_011515890.2:c.814+87C>T	XP_011514192.1:n.814+87C>T
XM_011515891.3:c.808+87C>T	XP_011514193.1:n.808+87C>T
XM_011515892.2:c.931+87C>T	XP_011514194.1:n.931+87C>T
XM_011515893.2:c.799+102C>T	XP_011514195.1:n.799+102C>T
XM_011515894.2:c.790+87C>T	XP_011514196.1:n.790+87C>T
XM_011515895.2:c.787+87C>T	XP_011514197.1:n.787+87C>T
XM_011515896.2:c.799+102C>T	XP_011514198.1:n.799+102C>T
XM_011515897.2:c.580+87C>T	XP_011514199.1:n.580+87C>T
XM_011515898.2:c.580+87C>T	XP_011514200.1:n.580+87C>T
XM_011515899.3:c.931+87C>T	XP_011514201.1:n.931+87C>T
XM_011515901.3:c.931+87C>T	XP_011514203.1:n.931+87C>T
XM_017011817.2:c.931+87C>T	XP_016867306.1:n.931+87C>T
XM_017011818.1:c.868+102C>T	XP_016867307.1:n.868+102C>T
XM_017011819.1:c.916+102C>T	XP_016867308.1:n.916+102C>T
XM_017011820.2:c.763+87C>T	XP_016867309.1:n.763+87C>T
XM_017011821.1:c.565+102C>T	XP_016867310.1:n.565+102C>T
XM_024446680.1:c.793+102C>T	XP_024302448.1:n.793+102C>T
XR_001744581.1:n.3546+87C>T
XR_002956413.1:n.3529+102C>T
XR_002956414.1:n.3546+87C>T
NM_001203247.2:c.892+102C>T	NP_001190176.1:n.892+102C>T
NM_001203248.2:c.865+102C>T	NP_001190177.1:n.865+102C>T
NM_001203249.2:c.865+102C>T	NP_001190178.1:n.865+102C>T
NM_004456.5:c.907+87C>T MANE Select	NP_004447.2:n.907+87C>T
NM_152998.3:c.775+102C>T	NP_694543.1:n.775+102C>T