Canonical Allele Identifier: CA2680645201

Gene: EPM2A EPM2A-DT

Linked Data

• gnomAD v4: 6-145735260-CGGCCCGGCTCCGCCCCGTCCTGCGCCGCCTCCTCGGCCGCCAGCTCCACCTCCCCGAGCCACA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.145735272_145735334del , CM000668.2:g.145735272_145735334del	GRCh38
NC_000006.11:g.146056408_146056470del , CM000668.1:g.146056408_146056470del	GRCh37
NC_000006.10:g.146098101_146098163del	NCBI36
NG_012832.1:g.5533_5595del
NG_012832.2:g.5533_5595del

Transcript Alleles

HGVS	Amino-acid change
ENST00000367519.9:c.176_238del (EPM2A) MANE Select	ENSP00000356489.3:p.Leu59_Gly79del
ENST00000435470.2:c.176_238del (EPM2A)	ENSP00000405913.2:p.Leu59_Gly79del
ENST00000611340.5:c.-114+673_-114+735del (EPM2A)	ENSP00000480268.1:n.-114+673_-114+735del
ENST00000638262.1:c.176_238del (EPM2A)	ENSP00000492876.1:p.Leu59_Gly79del
ENST00000639049.1:c.148_210del (EPM2A)
ENST00000639423.1:c.-114+585_-114+647del (EPM2A)	ENSP00000492701.1:n.-114+585_-114+647del
ENST00000639649.1:n.104_166del (EPM2A)
ENST00000640297.1:n.192_254del (EPM2A)
ENST00000640898.1:n.82+585_82+647del (EPM2A)
ENST00000640980.1:c.-114+585_-114+647del (EPM2A)	ENSP00000491191.1:n.-114+585_-114+647del
ENST00000367519.7:c.176_238del (EPM2A)	ENSP00000356489.3:p.Leu59_Gly79del
ENST00000618445.4:c.176_238del (EPM2A)	ENSP00000480339.1:p.Leu59_Gly79del
NM_001018041.1:c.176_238del (EPM2A)	NP_001018051.1:p.Leu59_Gly79del
NM_005670.3:c.176_238del (EPM2A)	NP_005661.1:p.Leu59_Gly79del
NR_038246.1:n.52+352_52+414del (EPM2A-DT)
XM_006715564.2:c.176_238del (EPM2A)	XP_006715627.1:p.Leu59_Gly79del
XM_011536113.1:c.176_238del (EPM2A)	XP_011534415.1:p.Leu59_Gly79del
XM_011536114.1:c.176_238del (EPM2A)	XP_011534416.1:p.Leu59_Gly79del
XM_011536115.1:c.176_238del (EPM2A)	XP_011534417.1:p.Leu59_Gly79del
NM_001360057.1:c.176_238del (EPM2A)	NP_001346986.1:p.Leu59_Gly79del
NM_001360064.1:c.-114+585_-114+647del (EPM2A)	NP_001346993.1:n.-114+585_-114+647del
NM_001360071.1:c.-494_-432del (EPM2A)	NP_001347000.1:n.-494_-432del
NR_153397.1:n.198_260del (EPM2A)
NR_153398.1:n.114+585_114+647del (EPM2A)
XM_011536113.2:c.176_238del (EPM2A)	XP_011534415.1:p.Leu59_Gly79del
XM_024446550.1:c.176_238del (EPM2A)	XP_024302318.1:p.Leu59_Gly79del
NM_005670.4:c.176_238del (EPM2A) MANE Select	NP_005661.1:p.Leu59_Gly79del
NM_001018041.2:c.176_238del (EPM2A)	NP_001018051.1:p.Leu59_Gly79del
NM_001360057.2:c.176_238del (EPM2A)	NP_001346986.1:p.Leu59_Gly79del
NM_001360064.2:c.-114+585_-114+647del (EPM2A)	NP_001346993.1:n.-114+585_-114+647del
NM_001360071.2:c.-494_-432del (EPM2A)	NP_001347000.1:n.-494_-432del
NM_001368129.2:c.-448_-386del (EPM2A)	NP_001355058.1:n.-448_-386del
NM_001368130.1:c.176_238del (EPM2A)	NP_001355059.1:p.Leu59_Gly79del
NM_001368131.1:c.-192_-130del (EPM2A)	NP_001355060.1:n.-192_-130del
NR_153398.2:n.116+585_116+647del (EPM2A)