Canonical Allele Identifier: CA366187926

Gene: EPM2A EPM2A-DT

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.145735241G>C , CM000668.2:g.145735241G>C	GRCh38
NC_000006.11:g.146056377G>C , CM000668.1:g.146056377G>C	GRCh37
NC_000006.10:g.146098070G>C	NCBI36
NG_012832.1:g.5615C>G
NG_012832.2:g.5615C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_005670.4:c.258C>G (EPM2A) MANE Select	NP_005661.1:p.Tyr86Ter
ENST00000367519.9:c.258C>G (EPM2A) MANE Select	ENSP00000356489.3:p.Tyr86Ter
NM_001018041.1:c.258C>G (EPM2A)	NP_001018051.1:p.Tyr86Ter
NM_001018041.2:c.258C>G (EPM2A)	NP_001018051.1:p.Tyr86Ter
NM_001360057.1:c.258C>G (EPM2A)	NP_001346986.1:p.Tyr86Ter
NM_001360057.2:c.258C>G (EPM2A)	NP_001346986.1:p.Tyr86Ter
NM_001360064.1:c.-114+667C>G (EPM2A)	NP_001346993.1:n.-114+667C>G
NM_001360064.2:c.-114+667C>G (EPM2A)	NP_001346993.1:n.-114+667C>G
NM_001360071.1:c.-412C>G (EPM2A)	NP_001347000.1:n.-412C>G
NM_001360071.2:c.-412C>G (EPM2A)	NP_001347000.1:n.-412C>G
NM_001368129.2:c.-366C>G (EPM2A)	NP_001355058.1:n.-366C>G
NM_001368130.1:c.258C>G (EPM2A)	NP_001355059.1:p.Tyr86Ter
NM_001368131.1:c.-114+4C>G (EPM2A)	NP_001355060.1:n.-114+4C>G
NM_005670.3:c.258C>G (EPM2A)	NP_005661.1:p.Tyr86Ter
NR_038246.1:n.52+321G>C (EPM2A-DT)
NR_153397.1:n.280C>G (EPM2A)
NR_153398.1:n.114+667C>G (EPM2A)
NR_153398.2:n.116+667C>G (EPM2A)
ENST00000367519.7:c.258C>G (EPM2A)	ENSP00000356489.3:p.Tyr86Ter
ENST00000435470.1:c.17C>G (EPM2A)
ENST00000435470.2:c.258C>G (EPM2A)	ENSP00000405913.2:p.Tyr86Ter
ENST00000611340.5:c.-114+755C>G (EPM2A)	ENSP00000480268.1:n.-114+755C>G
ENST00000618445.4:c.258C>G (EPM2A)	ENSP00000480339.1:p.Tyr86Ter
ENST00000638262.1:c.258C>G (EPM2A)	ENSP00000492876.1:p.Tyr86Ter
ENST00000638554.1:c.36C>G (EPM2A)	ENSP00000492823.1:p.Tyr12Ter
ENST00000638717.1:c.41C>G (EPM2A)
ENST00000639049.1:c.230C>G (EPM2A)
ENST00000639423.1:c.-114+667C>G (EPM2A)	ENSP00000492701.1:n.-114+667C>G
ENST00000639649.1:n.186C>G (EPM2A)
ENST00000640297.1:n.274C>G (EPM2A)
ENST00000640351.1:c.37+4C>G (EPM2A)
ENST00000640898.1:n.82+667C>G (EPM2A)
ENST00000640980.1:c.-114+667C>G (EPM2A)	ENSP00000491191.1:n.-114+667C>G
XM_006715564.2:c.258C>G (EPM2A)	XP_006715627.1:p.Tyr86Ter
XM_011536113.1:c.258C>G (EPM2A)	XP_011534415.1:p.Tyr86Ter
XM_011536113.2:c.258C>G (EPM2A)	XP_011534415.1:p.Tyr86Ter
XM_011536114.1:c.258C>G (EPM2A)	XP_011534416.1:p.Tyr86Ter
XM_011536115.1:c.258C>G (EPM2A)	XP_011534417.1:p.Tyr86Ter
XM_024446550.1:c.258C>G (EPM2A)	XP_024302318.1:p.Tyr86Ter