Canonical Allele Identifier: CA1751419095
Gene: EZH2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.148807377_148807383delinsAACAAGG , CM000669.2:g.148807377_148807383delinsAACAAGG GRCh38
NC_000007.13:g.148504469_148504475delinsAACAAGG , CM000669.1:g.148504469_148504475delinsAACAAGG GRCh37
NC_000007.12:g.148135402_148135408delinsAACAAGG NCBI36
NG_032043.1:g.81967_81973delinsCCTTGTT , LRG_531:g.81967_81973delinsCCTTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000683292.1:c.*1415_*1421delinsCCTTGTT ENSP00000507503.1:n.*1415_*1421delinsCCTTGTT
NM_001203247.1:c.*263_*269delinsCCTTGTT NP_001190176.1:n.*263_*269delinsCCTTGTT
NM_001203248.1:c.*263_*269delinsCCTTGTT NP_001190177.1:n.*263_*269delinsCCTTGTT
NM_001203249.1:c.*263_*269delinsCCTTGTT NP_001190178.1:n.*263_*269delinsCCTTGTT
NM_004456.4:c.*263_*269delinsCCTTGTT , LRG_531t1:c.*263_*269delinsCCTTGTT NP_004447.2:n.*263_*269delinsCCTTGTT
NM_152998.2:c.*263_*269delinsCCTTGTT NP_694543.1:n.*263_*269delinsCCTTGTT
XM_005249962.3:c.*263_*269delinsCCTTGTT XP_005250019.1:n.*263_*269delinsCCTTGTT
XM_005249963.3:c.*263_*269delinsCCTTGTT XP_005250020.1:n.*263_*269delinsCCTTGTT
XM_005249964.3:c.*263_*269delinsCCTTGTT XP_005250021.1:n.*263_*269delinsCCTTGTT
XM_011515883.1:c.*263_*269delinsCCTTGTT XP_011514185.1:n.*263_*269delinsCCTTGTT
XM_011515884.1:c.*263_*269delinsCCTTGTT XP_011514186.1:n.*263_*269delinsCCTTGTT
XM_011515885.1:c.*263_*269delinsCCTTGTT XP_011514187.1:n.*263_*269delinsCCTTGTT
XM_011515886.1:c.*263_*269delinsCCTTGTT XP_011514188.1:n.*263_*269delinsCCTTGTT
XM_011515887.1:c.*263_*269delinsCCTTGTT XP_011514189.1:n.*263_*269delinsCCTTGTT
XM_011515888.1:c.*263_*269delinsCCTTGTT XP_011514190.1:n.*263_*269delinsCCTTGTT
XM_011515889.1:c.*263_*269delinsCCTTGTT XP_011514191.1:n.*263_*269delinsCCTTGTT
XM_011515890.1:c.*263_*269delinsCCTTGTT XP_011514192.1:n.*263_*269delinsCCTTGTT
XM_011515891.1:c.*263_*269delinsCCTTGTT XP_011514193.1:n.*263_*269delinsCCTTGTT
XM_011515892.1:c.*263_*269delinsCCTTGTT XP_011514194.1:n.*263_*269delinsCCTTGTT
XM_011515893.1:c.*263_*269delinsCCTTGTT XP_011514195.1:n.*263_*269delinsCCTTGTT
XM_011515894.1:c.*263_*269delinsCCTTGTT XP_011514196.1:n.*263_*269delinsCCTTGTT
XM_011515895.1:c.*263_*269delinsCCTTGTT XP_011514197.1:n.*263_*269delinsCCTTGTT
XM_011515896.1:c.*263_*269delinsCCTTGTT XP_011514198.1:n.*263_*269delinsCCTTGTT
XM_011515897.1:c.*263_*269delinsCCTTGTT XP_011514199.1:n.*263_*269delinsCCTTGTT
XM_011515898.1:c.*263_*269delinsCCTTGTT XP_011514200.1:n.*263_*269delinsCCTTGTT
XR_928101.1:n.515+2292_515+2298delinsAACAAGG
XR_928102.1:n.722+2292_722+2298delinsAACAAGG
XM_005249962.4:c.*263_*269delinsCCTTGTT XP_005250019.1:n.*263_*269delinsCCTTGTT
XM_005249963.4:c.*263_*269delinsCCTTGTT XP_005250020.1:n.*263_*269delinsCCTTGTT
XM_005249964.4:c.*263_*269delinsCCTTGTT XP_005250021.1:n.*263_*269delinsCCTTGTT
XM_011515892.2:c.*263_*269delinsCCTTGTT XP_011514194.1:n.*263_*269delinsCCTTGTT
XM_011515893.2:c.*263_*269delinsCCTTGTT XP_011514195.1:n.*263_*269delinsCCTTGTT
XM_011515896.2:c.*263_*269delinsCCTTGTT XP_011514198.1:n.*263_*269delinsCCTTGTT
XM_017011818.1:c.*263_*269delinsCCTTGTT XP_016867307.1:n.*263_*269delinsCCTTGTT
XM_017011819.1:c.*263_*269delinsCCTTGTT XP_016867308.1:n.*263_*269delinsCCTTGTT
XM_017011821.1:c.*263_*269delinsCCTTGTT XP_016867310.1:n.*263_*269delinsCCTTGTT
XM_024446680.1:c.*263_*269delinsCCTTGTT XP_024302448.1:n.*263_*269delinsCCTTGTT
XR_002956413.1:n.5549_5555delinsCCTTGTT
XR_002956414.1:n.6009_6015delinsCCTTGTT