Canonical Allele Identifier: CA915944444

Gene: EPM2A EPM2A-DT

Linked Data

• ClinVar Variation Id: 665213
• ClinVar RCV Id: RCV000823447
• dbSNP Id: rs1583156284

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.145735292_145735293delinsGC , CM000668.2:g.145735292_145735293delinsGC	GRCh38
NC_000006.11:g.146056428_146056429delinsGC , CM000668.1:g.146056428_146056429delinsGC	GRCh37
NC_000006.10:g.146098121_146098122delinsGC	NCBI36
NG_012832.1:g.5563_5564delinsGC
NG_012832.2:g.5563_5564delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367519.9:c.206_207delinsGC (EPM2A) MANE Select	ENSP00000356489.3:p.Glu69Gly
ENST00000435470.2:c.206_207delinsGC (EPM2A)	ENSP00000405913.2:p.Glu69Gly
ENST00000611340.5:c.-114+703_-114+704delinsGC (EPM2A)	ENSP00000480268.1:n.-114+703_-114+704delinsGC
ENST00000638262.1:c.206_207delinsGC (EPM2A)	ENSP00000492876.1:p.Glu69Gly
ENST00000639049.1:c.178_179delinsGC (EPM2A)
ENST00000639423.1:c.-114+615_-114+616delinsGC (EPM2A)	ENSP00000492701.1:n.-114+615_-114+616delinsGC
ENST00000639649.1:n.134_135delinsGC (EPM2A)
ENST00000640297.1:n.222_223delinsGC (EPM2A)
ENST00000640898.1:n.82+615_82+616delinsGC (EPM2A)
ENST00000640980.1:c.-114+615_-114+616delinsGC (EPM2A)	ENSP00000491191.1:n.-114+615_-114+616delinsGC
ENST00000367519.7:c.206_207delinsGC (EPM2A)	ENSP00000356489.3:p.Glu69Gly
ENST00000618445.4:c.206_207delinsGC (EPM2A)	ENSP00000480339.1:p.Glu69Gly
NM_001018041.1:c.206_207delinsGC (EPM2A)	NP_001018051.1:p.Glu69Gly
NM_005670.3:c.206_207delinsGC (EPM2A)	NP_005661.1:p.Glu69Gly
NR_038246.1:n.52+372_52+373delinsGC (EPM2A-DT)
XM_006715564.2:c.206_207delinsGC (EPM2A)	XP_006715627.1:p.Glu69Gly
XM_011536113.1:c.206_207delinsGC (EPM2A)	XP_011534415.1:p.Glu69Gly
XM_011536114.1:c.206_207delinsGC (EPM2A)	XP_011534416.1:p.Glu69Gly
XM_011536115.1:c.206_207delinsGC (EPM2A)	XP_011534417.1:p.Glu69Gly
NM_001360057.1:c.206_207delinsGC (EPM2A)	NP_001346986.1:p.Glu69Gly
NM_001360064.1:c.-114+615_-114+616delinsGC (EPM2A)	NP_001346993.1:n.-114+615_-114+616delinsGC
NM_001360071.1:c.-464_-463delinsGC (EPM2A)	NP_001347000.1:n.-464_-463delinsGC
NR_153397.1:n.228_229delinsGC (EPM2A)
NR_153398.1:n.114+615_114+616delinsGC (EPM2A)
XM_011536113.2:c.206_207delinsGC (EPM2A)	XP_011534415.1:p.Glu69Gly
XM_024446550.1:c.206_207delinsGC (EPM2A)	XP_024302318.1:p.Glu69Gly
NM_005670.4:c.206_207delinsGC (EPM2A) MANE Select	NP_005661.1:p.Glu69Gly
NM_001018041.2:c.206_207delinsGC (EPM2A)	NP_001018051.1:p.Glu69Gly
NM_001360057.2:c.206_207delinsGC (EPM2A)	NP_001346986.1:p.Glu69Gly
NM_001360064.2:c.-114+615_-114+616delinsGC (EPM2A)	NP_001346993.1:n.-114+615_-114+616delinsGC
NM_001360071.2:c.-464_-463delinsGC (EPM2A)	NP_001347000.1:n.-464_-463delinsGC
NM_001368129.2:c.-418_-417delinsGC (EPM2A)	NP_001355058.1:n.-418_-417delinsGC
NM_001368130.1:c.206_207delinsGC (EPM2A)	NP_001355059.1:p.Glu69Gly
NM_001368131.1:c.-162_-161delinsGC (EPM2A)	NP_001355060.1:n.-162_-161delinsGC
NR_153398.2:n.116+615_116+616delinsGC (EPM2A)