Canonical Allele Identifier: CA2680645225

Gene: EPM2A EPM2A-DT

Linked Data

• gnomAD v4: 6-145735360-CCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.145735363_145735364del , CM000668.2:g.145735363_145735364del	GRCh38
NC_000006.11:g.146056499_146056500del , CM000668.1:g.146056499_146056500del	GRCh37
NC_000006.10:g.146098192_146098193del	NCBI36
NG_012832.1:g.5494_5495del
NG_012832.2:g.5494_5495del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367519.9:c.137_138del (EPM2A) MANE Select	ENSP00000356489.3:p.Ala46GlyfsTer?
ENST00000435470.2:c.137_138del (EPM2A)	ENSP00000405913.2:p.Ala46GlyfsTer?
ENST00000611340.5:c.-114+634_-114+635del (EPM2A)	ENSP00000480268.1:n.-114+634_-114+635del
ENST00000638262.1:c.137_138del (EPM2A)	ENSP00000492876.1:p.Ala46GlyfsTer?
ENST00000639049.1:c.109_110del (EPM2A)
ENST00000639423.1:c.-114+546_-114+547del (EPM2A)	ENSP00000492701.1:n.-114+546_-114+547del
ENST00000639649.1:n.65_66del (EPM2A)
ENST00000640297.1:n.153_154del (EPM2A)
ENST00000640898.1:n.82+546_82+547del (EPM2A)
ENST00000640980.1:c.-114+546_-114+547del (EPM2A)	ENSP00000491191.1:n.-114+546_-114+547del
ENST00000367519.7:c.137_138del (EPM2A)	ENSP00000356489.3:p.Ala46GlyfsTer?
ENST00000618445.4:c.137_138del (EPM2A)	ENSP00000480339.1:p.Ala46GlyfsTer?
NM_001018041.1:c.137_138del (EPM2A)	NP_001018051.1:p.Ala46GlyfsTer?
NM_005670.3:c.137_138del (EPM2A)	NP_005661.1:p.Ala46GlyfsTer?
NR_038246.1:n.52+443_52+444del (EPM2A-DT)
XM_006715564.2:c.137_138del (EPM2A)	XP_006715627.1:p.Ala46GlyfsTer?
XM_011536113.1:c.137_138del (EPM2A)	XP_011534415.1:p.Ala46GlyfsTer?
XM_011536114.1:c.137_138del (EPM2A)	XP_011534416.1:p.Ala46GlyfsTer?
XM_011536115.1:c.137_138del (EPM2A)	XP_011534417.1:p.Ala46GlyfsTer?
NM_001360057.1:c.137_138del (EPM2A)	NP_001346986.1:p.Ala46GlyfsTer?
NM_001360064.1:c.-114+546_-114+547del (EPM2A)	NP_001346993.1:n.-114+546_-114+547del
NM_001360071.1:c.-533_-532del (EPM2A)	NP_001347000.1:n.-533_-532del
NR_153397.1:n.159_160del (EPM2A)
NR_153398.1:n.114+546_114+547del (EPM2A)
XM_011536113.2:c.137_138del (EPM2A)	XP_011534415.1:p.Ala46GlyfsTer?
XM_024446550.1:c.137_138del (EPM2A)	XP_024302318.1:p.Ala46GlyfsTer?
NM_005670.4:c.137_138del (EPM2A) MANE Select	NP_005661.1:p.Ala46GlyfsTer?
NM_001018041.2:c.137_138del (EPM2A)	NP_001018051.1:p.Ala46GlyfsTer?
NM_001360057.2:c.137_138del (EPM2A)	NP_001346986.1:p.Ala46GlyfsTer?
NM_001360064.2:c.-114+546_-114+547del (EPM2A)	NP_001346993.1:n.-114+546_-114+547del
NM_001360071.2:c.-533_-532del (EPM2A)	NP_001347000.1:n.-533_-532del
NM_001368129.2:c.-487_-486del (EPM2A)	NP_001355058.1:n.-487_-486del
NM_001368130.1:c.137_138del (EPM2A)	NP_001355059.1:p.Ala46GlyfsTer?
NM_001368131.1:c.-231_-230del (EPM2A)	NP_001355060.1:n.-231_-230del
NR_153398.2:n.116+546_116+547del (EPM2A)