Canonical Allele Identifier: CA369711786

Gene: EZH2

Linked Data

• MyVariant Identifiers: chr7:g.148504763A>G (hg19) ; chr7:g.148807671A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.148807671A>G , CM000669.2:g.148807671A>G	GRCh38
NC_000007.13:g.148504763A>G , CM000669.1:g.148504763A>G	GRCh37
NC_000007.12:g.148135696A>G	NCBI36
NG_032043.1:g.81679T>C , LRG_531:g.81679T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682263.1:n.4131T>C
ENST00000682317.1:c.*1293T>C	ENSP00000508286.1:n.*1293T>C
ENST00000683292.1:c.*1127T>C	ENSP00000507503.1:n.*1127T>C
ENST00000683293.1:n.3950T>C
ENST00000683744.1:c.*1293T>C	ENSP00000506949.1:n.*1293T>C
ENST00000684300.1:c.*1293T>C	ENSP00000508407.1:n.*1293T>C
ENST00000684400.1:n.4218T>C
ENST00000684436.1:n.2547T>C
ENST00000684510.1:n.2609T>C
ENST00000320356.7:c.2231T>C MANE Select	ENSP00000320147.2:p.Ile744Thr
ENST00000320356.6:c.2231T>C	ENSP00000320147.2:p.Ile744Thr
ENST00000350995.6:c.2099T>C	ENSP00000223193.2:p.Ile700Thr
ENST00000460911.5:c.2216T>C	ENSP00000419711.1:p.Ile739Thr
ENST00000476773.5:c.2063T>C	ENSP00000419050.1:p.Ile688Thr
ENST00000478654.5:c.2063T>C	ENSP00000417062.1:p.Ile688Thr
ENST00000483967.5:c.2189T>C	ENSP00000419856.1:p.Ile730Thr
ENST00000492143.5:c.*2221T>C	ENSP00000417377.1:n.*2221T>C
NM_001203247.1:c.2216T>C	NP_001190176.1:p.Ile739Thr
NM_001203248.1:c.2189T>C	NP_001190177.1:p.Ile730Thr
NM_001203249.1:c.2063T>C	NP_001190178.1:p.Ile688Thr
NM_004456.4:c.2231T>C , LRG_531t1:c.2231T>C	NP_004447.2:p.Ile744Thr
NM_152998.2:c.2099T>C	NP_694543.1:p.Ile700Thr
XM_005249962.3:c.2240T>C	XP_005250019.1:p.Ile747Thr
XM_005249963.3:c.2213T>C	XP_005250020.1:p.Ile738Thr
XM_005249964.3:c.2087T>C	XP_005250021.1:p.Ile696Thr
XM_011515883.1:c.2255T>C	XP_011514185.1:p.Ile752Thr
XM_011515884.1:c.2231T>C	XP_011514186.1:p.Ile744Thr
XM_011515885.1:c.2228T>C	XP_011514187.1:p.Ile743Thr
XM_011515886.1:c.2207T>C	XP_011514188.1:p.Ile736Thr
XM_011515887.1:c.2204T>C	XP_011514189.1:p.Ile735Thr
XM_011515888.1:c.2204T>C	XP_011514190.1:p.Ile735Thr
XM_011515889.1:c.2165T>C	XP_011514191.1:p.Ile722Thr
XM_011515890.1:c.2138T>C	XP_011514192.1:p.Ile713Thr
XM_011515891.1:c.2132T>C	XP_011514193.1:p.Ile711Thr
XM_011515892.1:c.2129T>C	XP_011514194.1:p.Ile710Thr
XM_011515893.1:c.2123T>C	XP_011514195.1:p.Ile708Thr
XM_011515894.1:c.2114T>C	XP_011514196.1:p.Ile705Thr
XM_011515895.1:c.2111T>C	XP_011514197.1:p.Ile704Thr
XM_011515896.1:c.1997T>C	XP_011514198.1:p.Ile666Thr
XM_011515897.1:c.1904T>C	XP_011514199.1:p.Ile635Thr
XM_011515898.1:c.1904T>C	XP_011514200.1:p.Ile635Thr
XR_928101.1:n.515+2586A>G
XR_928102.1:n.722+2586A>G
XM_005249962.4:c.2240T>C	XP_005250019.1:p.Ile747Thr
XM_005249963.4:c.2213T>C	XP_005250020.1:p.Ile738Thr
XM_005249964.4:c.2087T>C	XP_005250021.1:p.Ile696Thr
XM_011515883.2:c.2255T>C	XP_011514185.1:p.Ile752Thr
XM_011515884.2:c.2231T>C	XP_011514186.1:p.Ile744Thr
XM_011515885.2:c.2228T>C	XP_011514187.1:p.Ile743Thr
XM_011515886.2:c.2207T>C	XP_011514188.1:p.Ile736Thr
XM_011515887.3:c.2204T>C	XP_011514189.1:p.Ile735Thr
XM_011515888.2:c.2204T>C	XP_011514190.1:p.Ile735Thr
XM_011515889.2:c.2165T>C	XP_011514191.1:p.Ile722Thr
XM_011515890.2:c.2138T>C	XP_011514192.1:p.Ile713Thr
XM_011515891.3:c.2132T>C	XP_011514193.1:p.Ile711Thr
XM_011515892.2:c.2129T>C	XP_011514194.1:p.Ile710Thr
XM_011515893.2:c.2123T>C	XP_011514195.1:p.Ile708Thr
XM_011515894.2:c.2114T>C	XP_011514196.1:p.Ile705Thr
XM_011515895.2:c.2111T>C	XP_011514197.1:p.Ile704Thr
XM_011515896.2:c.1997T>C	XP_011514198.1:p.Ile666Thr
XM_011515897.2:c.1904T>C	XP_011514199.1:p.Ile635Thr
XM_011515898.2:c.1904T>C	XP_011514200.1:p.Ile635Thr
XM_017011817.2:c.2255T>C	XP_016867306.1:p.Ile752Thr
XM_017011818.1:c.2192T>C	XP_016867307.1:p.Ile731Thr
XM_017011819.1:c.2114T>C	XP_016867308.1:p.Ile705Thr
XM_017011820.2:c.2087T>C	XP_016867309.1:p.Ile696Thr
XM_017011821.1:c.1889T>C	XP_016867310.1:p.Ile630Thr
XM_024446680.1:c.2117T>C	XP_024302448.1:p.Ile706Thr
XR_001744581.1:n.4605T>C
XR_002956413.1:n.5261T>C
XR_002956414.1:n.5721T>C
NM_001203247.2:c.2216T>C	NP_001190176.1:p.Ile739Thr
NM_001203248.2:c.2189T>C	NP_001190177.1:p.Ile730Thr
NM_001203249.2:c.2063T>C	NP_001190178.1:p.Ile688Thr
NM_004456.5:c.2231T>C MANE Select	NP_004447.2:p.Ile744Thr
NM_152998.3:c.2099T>C	NP_694543.1:p.Ile700Thr