Canonical Allele Identifier: CA366191445
Gene: EPM2A HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.145635415T>C , CM000668.2:g.145635415T>C GRCh38
NC_000006.11:g.145956551T>C , CM000668.1:g.145956551T>C GRCh37
NC_000006.10:g.145998244T>C NCBI36
NG_012832.1:g.105441A>G
NG_012832.2:g.105441A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367519.9:c.548A>G MANE Select ENSP00000356489.3:p.Glu183Gly
ENST00000435470.2:c.548A>G ENSP00000405913.2:p.Glu183Gly
ENST00000450221.6:c.170A>G ENSP00000414900.2:p.Glu57Gly
ENST00000496228.2:n.516A>G
ENST00000611340.5:c.134A>G ENSP00000480268.1:p.Glu45Gly
ENST00000638262.1:c.477-7722A>G ENSP00000492876.1:n.477-7722A>G
ENST00000638554.1:c.487A>G ENSP00000492823.1:n.487A>G
ENST00000638717.1:c.331A>G
ENST00000638778.1:c.134A>G ENSP00000491353.1:p.Glu45Gly
ENST00000638783.1:c.134A>G ENSP00000491338.1:p.Glu45Gly
ENST00000639049.1:c.775A>G
ENST00000639423.1:c.134A>G ENSP00000492701.1:p.Glu45Gly
ENST00000639465.1:c.134A>G ENSP00000491180.1:p.Glu45Gly
ENST00000639648.1:n.129A>G
ENST00000639799.1:n.1089A>G
ENST00000639849.1:c.*82A>G ENSP00000491224.1:n.*82A>G
ENST00000639859.1:n.5872A>G
ENST00000640225.1:c.*82A>G ENSP00000492179.1:n.*82A>G
ENST00000640351.1:c.284A>G
ENST00000640980.1:c.63-7722A>G ENSP00000491191.1:n.63-7722A>G
ENST00000367519.7:c.548A>G ENSP00000356489.3:p.Glu183Gly
ENST00000435470.1:c.307A>G
ENST00000450221.5:c.247A>G
ENST00000489412.1:n.167A>G
ENST00000496228.1:n.442A>G
ENST00000611340.4:c.134A>G ENSP00000480268.1:p.Glu45Gly
ENST00000618445.4:c.548A>G ENSP00000480339.1:p.Glu183Gly
NM_001018041.1:c.548A>G NP_001018051.1:p.Glu183Gly
NM_005670.3:c.548A>G NP_005661.1:p.Glu183Gly
XM_006715564.2:c.477-7722A>G XP_006715627.1:n.477-7722A>G
XM_011536113.1:c.548A>G XP_011534415.1:p.Glu183Gly
XM_011536114.1:c.548A>G XP_011534416.1:p.Glu183Gly
XM_011536116.1:c.134A>G XP_011534418.1:p.Glu45Gly
NM_001360057.1:c.477-7722A>G NP_001346986.1:n.477-7722A>G
NM_001360064.1:c.134A>G NP_001346993.1:p.Glu45Gly
NM_001360071.1:c.134A>G NP_001347000.1:p.Glu45Gly
NR_153397.1:n.731A>G
NR_153398.1:n.290-7722A>G
XM_011536113.2:c.548A>G XP_011534415.1:p.Glu183Gly
XM_017011301.1:c.86A>G XP_016866790.1:p.Glu29Gly
XM_017011302.1:c.86A>G XP_016866791.1:p.Glu29Gly
XM_024446550.1:c.548A>G XP_024302318.1:p.Glu183Gly
XM_024446551.1:c.134A>G XP_024302319.1:p.Glu45Gly
NM_005670.4:c.548A>G MANE Select NP_005661.1:p.Glu183Gly
NM_001018041.2:c.548A>G NP_001018051.1:p.Glu183Gly
NM_001360057.2:c.477-7722A>G NP_001346986.1:n.477-7722A>G
NM_001360064.2:c.134A>G NP_001346993.1:p.Glu45Gly
NM_001360071.2:c.134A>G NP_001347000.1:p.Glu45Gly
NM_001368129.2:c.86A>G NP_001355058.1:p.Glu29Gly
NM_001368130.1:c.548A>G NP_001355059.1:p.Glu183Gly
NM_001368131.1:c.134A>G NP_001355060.1:p.Glu45Gly
NM_001368132.1:c.86A>G NP_001355061.1:p.Glu29Gly
NR_153398.2:n.292-7722A>G