Canonical Allele Identifier: CA366188103
Gene: EPM2A HGNC NCBI
EPM2A-DT HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.145735321A>C , CM000668.2:g.145735321A>C GRCh38
NC_000006.11:g.146056457A>C , CM000668.1:g.146056457A>C GRCh37
NC_000006.10:g.146098150A>C NCBI36
NG_012832.1:g.5535T>G
NG_012832.2:g.5535T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367519.9:c.178T>G (EPM2A) MANE Select ENSP00000356489.3:p.Trp60Gly
ENST00000435470.2:c.178T>G (EPM2A) ENSP00000405913.2:p.Trp60Gly
ENST00000611340.5:c.-114+675T>G (EPM2A) ENSP00000480268.1:n.-114+675T>G
ENST00000638262.1:c.178T>G (EPM2A) ENSP00000492876.1:p.Trp60Gly
ENST00000639049.1:c.150T>G (EPM2A)
ENST00000639423.1:c.-114+587T>G (EPM2A) ENSP00000492701.1:n.-114+587T>G
ENST00000639649.1:n.106T>G (EPM2A)
ENST00000640297.1:n.194T>G (EPM2A)
ENST00000640898.1:n.82+587T>G (EPM2A)
ENST00000640980.1:c.-114+587T>G (EPM2A) ENSP00000491191.1:n.-114+587T>G
ENST00000367519.7:c.178T>G (EPM2A) ENSP00000356489.3:p.Trp60Gly
ENST00000618445.4:c.178T>G (EPM2A) ENSP00000480339.1:p.Trp60Gly
NM_001018041.1:c.178T>G (EPM2A) NP_001018051.1:p.Trp60Gly
NM_005670.3:c.178T>G (EPM2A) NP_005661.1:p.Trp60Gly
NR_038246.1:n.52+401A>C (EPM2A-DT)
XM_006715564.2:c.178T>G (EPM2A) XP_006715627.1:p.Trp60Gly
XM_011536113.1:c.178T>G (EPM2A) XP_011534415.1:p.Trp60Gly
XM_011536114.1:c.178T>G (EPM2A) XP_011534416.1:p.Trp60Gly
XM_011536115.1:c.178T>G (EPM2A) XP_011534417.1:p.Trp60Gly
NM_001360057.1:c.178T>G (EPM2A) NP_001346986.1:p.Trp60Gly
NM_001360064.1:c.-114+587T>G (EPM2A) NP_001346993.1:n.-114+587T>G
NM_001360071.1:c.-492T>G (EPM2A) NP_001347000.1:n.-492T>G
NR_153397.1:n.200T>G (EPM2A)
NR_153398.1:n.114+587T>G (EPM2A)
XM_011536113.2:c.178T>G (EPM2A) XP_011534415.1:p.Trp60Gly
XM_024446550.1:c.178T>G (EPM2A) XP_024302318.1:p.Trp60Gly
NM_005670.4:c.178T>G (EPM2A) MANE Select NP_005661.1:p.Trp60Gly
NM_001018041.2:c.178T>G (EPM2A) NP_001018051.1:p.Trp60Gly
NM_001360057.2:c.178T>G (EPM2A) NP_001346986.1:p.Trp60Gly
NM_001360064.2:c.-114+587T>G (EPM2A) NP_001346993.1:n.-114+587T>G
NM_001360071.2:c.-492T>G (EPM2A) NP_001347000.1:n.-492T>G
NM_001368129.2:c.-446T>G (EPM2A) NP_001355058.1:n.-446T>G
NM_001368130.1:c.178T>G (EPM2A) NP_001355059.1:p.Trp60Gly
NM_001368131.1:c.-190T>G (EPM2A) NP_001355060.1:n.-190T>G
NR_153398.2:n.116+587T>G (EPM2A)