Canonical Allele Identifier: CA366191572

Gene: EPM2A

Linked Data

• COSMIC: COSM304790
• MyVariant Identifiers: chr6:g.145956608A>C (hg19) ; chr6:g.145635472A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.145635472A>C , CM000668.2:g.145635472A>C	GRCh38
NC_000006.11:g.145956608A>C , CM000668.1:g.145956608A>C	GRCh37
NC_000006.10:g.145998301A>C	NCBI36
NG_012832.1:g.105384T>G
NG_012832.2:g.105384T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367519.9:c.491T>G MANE Select	ENSP00000356489.3:p.Ile164Ser
ENST00000435470.2:c.491T>G	ENSP00000405913.2:p.Ile164Ser
ENST00000450221.6:c.113T>G	ENSP00000414900.2:p.Ile38Ser
ENST00000496228.2:n.459T>G
ENST00000611340.5:c.77T>G	ENSP00000480268.1:p.Ile26Ser
ENST00000638262.1:c.477-7779T>G	ENSP00000492876.1:n.477-7779T>G
ENST00000638554.1:c.430T>G	ENSP00000492823.1:n.430T>G
ENST00000638717.1:c.274T>G
ENST00000638778.1:c.77T>G	ENSP00000491353.1:p.Ile26Ser
ENST00000638783.1:c.77T>G	ENSP00000491338.1:p.Ile26Ser
ENST00000639049.1:c.718T>G
ENST00000639423.1:c.77T>G	ENSP00000492701.1:p.Ile26Ser
ENST00000639465.1:c.77T>G	ENSP00000491180.1:p.Ile26Ser
ENST00000639648.1:n.72T>G
ENST00000639799.1:n.1032T>G
ENST00000639849.1:c.*25T>G	ENSP00000491224.1:n.*25T>G
ENST00000639859.1:n.5815T>G
ENST00000640225.1:c.*25T>G	ENSP00000492179.1:n.*25T>G
ENST00000640297.1:n.332T>G
ENST00000640351.1:c.227T>G
ENST00000640980.1:c.63-7779T>G	ENSP00000491191.1:n.63-7779T>G
ENST00000367519.7:c.491T>G	ENSP00000356489.3:p.Ile164Ser
ENST00000435470.1:c.250T>G
ENST00000450221.5:c.190T>G
ENST00000489412.1:n.110T>G
ENST00000496228.1:n.385T>G
ENST00000611340.4:c.77T>G	ENSP00000480268.1:p.Ile26Ser
ENST00000618445.4:c.491T>G	ENSP00000480339.1:p.Ile164Ser
NM_001018041.1:c.491T>G	NP_001018051.1:p.Ile164Ser
NM_005670.3:c.491T>G	NP_005661.1:p.Ile164Ser
XM_006715564.2:c.477-7779T>G	XP_006715627.1:n.477-7779T>G
XM_011536113.1:c.491T>G	XP_011534415.1:p.Ile164Ser
XM_011536114.1:c.491T>G	XP_011534416.1:p.Ile164Ser
XM_011536116.1:c.77T>G	XP_011534418.1:p.Ile26Ser
NM_001360057.1:c.477-7779T>G	NP_001346986.1:n.477-7779T>G
NM_001360064.1:c.77T>G	NP_001346993.1:p.Ile26Ser
NM_001360071.1:c.77T>G	NP_001347000.1:p.Ile26Ser
NR_153397.1:n.674T>G
NR_153398.1:n.290-7779T>G
XM_011536113.2:c.491T>G	XP_011534415.1:p.Ile164Ser
XM_017011301.1:c.29T>G	XP_016866790.1:p.Ile10Ser
XM_017011302.1:c.29T>G	XP_016866791.1:p.Ile10Ser
XM_024446550.1:c.491T>G	XP_024302318.1:p.Ile164Ser
XM_024446551.1:c.77T>G	XP_024302319.1:p.Ile26Ser
NM_005670.4:c.491T>G MANE Select	NP_005661.1:p.Ile164Ser
NM_001018041.2:c.491T>G	NP_001018051.1:p.Ile164Ser
NM_001360057.2:c.477-7779T>G	NP_001346986.1:n.477-7779T>G
NM_001360064.2:c.77T>G	NP_001346993.1:p.Ile26Ser
NM_001360071.2:c.77T>G	NP_001347000.1:p.Ile26Ser
NM_001368129.2:c.29T>G	NP_001355058.1:p.Ile10Ser
NM_001368130.1:c.491T>G	NP_001355059.1:p.Ile164Ser
NM_001368131.1:c.77T>G	NP_001355060.1:p.Ile26Ser
NM_001368132.1:c.29T>G	NP_001355061.1:p.Ile10Ser
NR_153398.2:n.292-7779T>G