Canonical Allele Identifier: CA423435564
Gene: ESRRG HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.216519327C>A , CM000663.2:g.216519327C>A GRCh38
NC_000001.10:g.216692669C>A , CM000663.1:g.216692669C>A GRCh37
NC_000001.9:g.214759292C>A NCBI36
NG_029784.1:g.623429G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000408911.8:c.957G>T MANE Select ENSP00000386171.3:p.Ser319=
ENST00000673908.1:c.909G>T ENSP00000500992.1:p.Ser303=
ENST00000359162.6:c.888G>T ENSP00000352077.2:p.Ser296=
ENST00000360012.7:c.888G>T ENSP00000353108.3:p.Ser296=
ENST00000361395.6:c.888G>T ENSP00000354584.2:p.Ser296=
ENST00000361525.7:c.888G>T ENSP00000355225.3:p.Ser296=
ENST00000366937.5:c.993G>T ENSP00000355904.1:p.Ser331=
ENST00000366938.6:c.888G>T ENSP00000355905.2:p.Ser296=
ENST00000366940.6:c.888G>T ENSP00000355907.2:p.Ser296=
ENST00000391890.7:c.888G>T ENSP00000375761.4:p.Ser296=
ENST00000408911.7:c.957G>T ENSP00000386171.3:p.Ser319=
ENST00000463665.5:c.771G>T ENSP00000418629.1:p.Ser257=
ENST00000475275.5:c.888G>T ENSP00000419514.1:p.Ser296=
ENST00000487276.5:c.888G>T ENSP00000419155.1:p.Ser296=
ENST00000493603.5:c.888G>T ENSP00000419594.1:p.Ser296=
ENST00000493748.5:c.888G>T ENSP00000417374.1:p.Ser296=
ENST00000616180.4:c.888G>T ENSP00000481528.1:p.Ser296=
NM_001134285.2:c.888G>T NP_001127757.1:p.Ser296=
NM_001243505.1:c.204G>T NP_001230434.1:p.Ser68=
NM_001243506.1:c.402G>T NP_001230435.1:p.Ser134=
NM_001243507.1:c.771G>T NP_001230436.1:p.Ser257=
NM_001243509.1:c.888G>T NP_001230438.1:p.Ser296=
NM_001243510.2:c.888G>T NP_001230439.1:p.Ser296=
NM_001243511.2:c.888G>T NP_001230440.1:p.Ser296=
NM_001243512.1:c.888G>T NP_001230441.1:p.Ser296=
NM_001243513.1:c.888G>T NP_001230442.1:p.Ser296=
NM_001243514.1:c.888G>T NP_001230443.1:p.Ser296=
NM_001243515.1:c.888G>T NP_001230444.1:p.Ser296=
NM_001243518.1:c.993G>T NP_001230447.1:p.Ser331=
NM_001243519.1:c.888G>T NP_001230448.1:p.Ser296=
NM_001438.3:c.957G>T NP_001429.2:p.Ser319=
NM_206594.2:c.888G>T NP_996317.1:p.Ser296=
NM_206595.2:c.888G>T NP_996318.1:p.Ser296=
XM_006711205.1:c.888G>T XP_006711268.1:p.Ser296=
XM_011509265.1:c.1014G>T XP_011507567.1:p.Ser338=
XM_011509266.1:c.993G>T XP_011507568.1:p.Ser331=
XM_011509267.1:c.993G>T XP_011507569.1:p.Ser331=
XM_011509268.1:c.993G>T XP_011507570.1:p.Ser331=
XM_011509269.1:c.993G>T XP_011507571.1:p.Ser331=
XM_011509270.1:c.978G>T XP_011507572.1:p.Ser326=
XM_011509271.1:c.924G>T XP_011507573.1:p.Ser308=
XM_011509272.1:c.924G>T XP_011507574.1:p.Ser308=
XM_011509273.1:c.909G>T XP_011507575.1:p.Ser303=
XM_011509274.1:c.909G>T XP_011507576.1:p.Ser303=
XM_011509275.1:c.909G>T XP_011507577.1:p.Ser303=
XM_011509276.1:c.909G>T XP_011507578.1:p.Ser303=
XM_011509277.1:c.909G>T XP_011507579.1:p.Ser303=
XM_011509278.1:c.909G>T XP_011507580.1:p.Ser303=
XM_011509279.1:c.909G>T XP_011507581.1:p.Ser303=
XM_011509280.1:c.909G>T XP_011507582.1:p.Ser303=
XM_011509281.1:c.909G>T XP_011507583.1:p.Ser303=
XM_011509282.1:c.909G>T XP_011507584.1:p.Ser303=
NM_001350122.1:c.888G>T NP_001337051.1:p.Ser296=
NM_001350123.1:c.888G>T NP_001337052.1:p.Ser296=
NM_001350124.1:c.888G>T NP_001337053.1:p.Ser296=
NM_001350125.1:c.888G>T NP_001337054.1:p.Ser296=
XM_011509265.3:c.1014G>T XP_011507567.1:p.Ser338=
XM_011509266.3:c.993G>T XP_011507568.1:p.Ser331=
XM_011509268.2:c.993G>T XP_011507570.1:p.Ser331=
XM_011509269.2:c.993G>T XP_011507571.1:p.Ser331=
XM_011509271.2:c.924G>T XP_011507573.1:p.Ser308=
XM_011509280.2:c.909G>T XP_011507582.1:p.Ser303=
XM_017000621.2:c.1014G>T XP_016856110.1:p.Ser338=
XM_017000622.1:c.1014G>T XP_016856111.1:p.Ser338=
XM_017000623.2:c.1014G>T XP_016856112.1:p.Ser338=
XM_017000624.2:c.1014G>T XP_016856113.1:p.Ser338=
XM_017000625.1:c.1014G>T XP_016856114.1:p.Ser338=
XM_017000626.1:c.972G>T XP_016856115.1:p.Ser324=
XM_017000627.1:c.972G>T XP_016856116.1:p.Ser324=
XM_017000628.1:c.966G>T XP_016856117.1:p.Ser322=
XM_017000630.1:c.924G>T XP_016856119.1:p.Ser308=
XM_017000631.2:c.909G>T XP_016856120.1:p.Ser303=
XM_017000632.2:c.909G>T XP_016856121.1:p.Ser303=
XM_017000633.1:c.909G>T XP_016856122.1:p.Ser303=
XM_017000634.2:c.909G>T XP_016856123.1:p.Ser303=
XM_017000635.1:c.909G>T XP_016856124.1:p.Ser303=
XM_017000636.2:c.909G>T XP_016856125.1:p.Ser303=
XM_017000637.1:c.909G>T XP_016856126.1:p.Ser303=
XM_017000638.2:c.888G>T XP_016856127.1:p.Ser296=
XM_017000639.1:c.888G>T XP_016856128.1:p.Ser296=
XM_017000641.1:c.888G>T XP_016856130.1:p.Ser296=
XM_017000644.1:c.888G>T XP_016856133.1:p.Ser296=
XM_017000645.1:c.888G>T XP_016856134.1:p.Ser296=
XM_024453959.1:c.909G>T XP_024309727.1:p.Ser303=
XM_024453960.1:c.909G>T XP_024309728.1:p.Ser303=
XM_024453975.1:c.888G>T XP_024309743.1:p.Ser296=
XM_024453979.1:c.888G>T XP_024309747.1:p.Ser296=
XM_024453980.1:c.888G>T XP_024309748.1:p.Ser296=
NM_001438.4:c.957G>T MANE Select NP_001429.2:p.Ser319=
NM_001134285.3:c.888G>T NP_001127757.1:p.Ser296=
NM_001243505.2:c.204G>T NP_001230434.1:p.Ser68=
NM_001243506.2:c.402G>T NP_001230435.1:p.Ser134=
NM_001243507.2:c.771G>T NP_001230436.1:p.Ser257=
NM_001243509.2:c.888G>T NP_001230438.1:p.Ser296=
NM_001243510.3:c.888G>T NP_001230439.1:p.Ser296=
NM_001243511.3:c.888G>T NP_001230440.1:p.Ser296=
NM_001243514.2:c.888G>T NP_001230443.1:p.Ser296=
NM_001243515.2:c.888G>T NP_001230444.1:p.Ser296=
NM_001243518.2:c.993G>T NP_001230447.1:p.Ser331=
NM_001350122.2:c.888G>T NP_001337051.1:p.Ser296=
NM_001350123.2:c.888G>T NP_001337052.1:p.Ser296=
NM_001350124.2:c.888G>T NP_001337053.1:p.Ser296=
NM_001350125.2:c.888G>T NP_001337054.1:p.Ser296=
NM_206595.3:c.888G>T NP_996318.1:p.Ser296=
NM_001243519.2:c.888G>T NP_001230448.1:p.Ser296=
NM_206594.3:c.888G>T NP_996317.1:p.Ser296=
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