Canonical Allele Identifier: CA820265122

Gene: EPM2A

Linked Data

• dbSNP Id: rs1214182629
• MyVariant Identifiers: chr6:g.145956846_145956847del (hg19) ; chr6:g.145635710_145635711del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.145635710_145635711del , CM000668.2:g.145635710_145635711del	GRCh38
NC_000006.11:g.145956846_145956847del , CM000668.1:g.145956846_145956847del	GRCh37
NC_000006.10:g.145998539_145998540del	NCBI36
NG_012832.1:g.105145_105146del
NG_012832.2:g.105145_105146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367519.9:c.477-225_477-224del MANE Select	ENSP00000356489.3:n.477-225_477-224del
ENST00000435470.2:c.477-225_477-224del	ENSP00000405913.2:n.477-225_477-224del
ENST00000450221.6:c.99-225_99-224del	ENSP00000414900.2:n.99-225_99-224del
ENST00000496228.2:n.445-225_445-224del
ENST00000611340.5:c.63-225_63-224del	ENSP00000480268.1:n.63-225_63-224del
ENST00000638262.1:c.477-8018_477-8017del	ENSP00000492876.1:n.477-8018_477-8017del
ENST00000638554.1:c.416-225_416-224del	ENSP00000492823.1:n.416-225_416-224del
ENST00000638717.1:c.260-225_260-224del
ENST00000638778.1:c.63-225_63-224del	ENSP00000491353.1:n.63-225_63-224del
ENST00000638783.1:c.63-225_63-224del	ENSP00000491338.1:n.63-225_63-224del
ENST00000639049.1:c.704-225_704-224del
ENST00000639423.1:c.63-225_63-224del	ENSP00000492701.1:n.63-225_63-224del
ENST00000639465.1:c.63-225_63-224del	ENSP00000491180.1:n.63-225_63-224del
ENST00000639648.1:n.58-225_58-224del
ENST00000639799.1:n.1018-225_1018-224del
ENST00000639849.1:c.*11-225_*11-224del	ENSP00000491224.1:n.*11-225_*11-224del
ENST00000639859.1:n.5576_5577del
ENST00000640225.1:c.*11-225_*11-224del	ENSP00000492179.1:n.*11-225_*11-224del
ENST00000640297.1:n.318-225_318-224del
ENST00000640351.1:c.213-225_213-224del
ENST00000640980.1:c.63-8018_63-8017del	ENSP00000491191.1:n.63-8018_63-8017del
ENST00000367519.7:c.477-225_477-224del	ENSP00000356489.3:n.477-225_477-224del
ENST00000435470.1:c.236-225_236-224del
ENST00000450221.5:c.176-225_176-224del
ENST00000489412.1:n.96-225_96-224del
ENST00000496228.1:n.371-225_371-224del
ENST00000611340.4:c.63-225_63-224del	ENSP00000480268.1:n.63-225_63-224del
ENST00000618445.4:c.477-225_477-224del	ENSP00000480339.1:n.477-225_477-224del
NM_001018041.1:c.477-225_477-224del	NP_001018051.1:n.477-225_477-224del
NM_005670.3:c.477-225_477-224del	NP_005661.1:n.477-225_477-224del
XM_006715564.2:c.477-8018_477-8017del	XP_006715627.1:n.477-8018_477-8017del
XM_011536113.1:c.477-225_477-224del	XP_011534415.1:n.477-225_477-224del
XM_011536114.1:c.477-225_477-224del	XP_011534416.1:n.477-225_477-224del
XM_011536116.1:c.63-225_63-224del	XP_011534418.1:n.63-225_63-224del
NM_001360057.1:c.477-8018_477-8017del	NP_001346986.1:n.477-8018_477-8017del
NM_001360064.1:c.63-225_63-224del	NP_001346993.1:n.63-225_63-224del
NM_001360071.1:c.63-225_63-224del	NP_001347000.1:n.63-225_63-224del
NR_153397.1:n.660-225_660-224del
NR_153398.1:n.290-8018_290-8017del
XM_011536113.2:c.477-225_477-224del	XP_011534415.1:n.477-225_477-224del
XM_017011301.1:c.15-225_15-224del	XP_016866790.1:n.15-225_15-224del
XM_017011302.1:c.15-225_15-224del	XP_016866791.1:n.15-225_15-224del
XM_024446550.1:c.477-225_477-224del	XP_024302318.1:n.477-225_477-224del
XM_024446551.1:c.63-225_63-224del	XP_024302319.1:n.63-225_63-224del
NM_005670.4:c.477-225_477-224del MANE Select	NP_005661.1:n.477-225_477-224del
NM_001018041.2:c.477-225_477-224del	NP_001018051.1:n.477-225_477-224del
NM_001360057.2:c.477-8018_477-8017del	NP_001346986.1:n.477-8018_477-8017del
NM_001360064.2:c.63-225_63-224del	NP_001346993.1:n.63-225_63-224del
NM_001360071.2:c.63-225_63-224del	NP_001347000.1:n.63-225_63-224del
NM_001368129.2:c.15-225_15-224del	NP_001355058.1:n.15-225_15-224del
NM_001368130.1:c.477-225_477-224del	NP_001355059.1:n.477-225_477-224del
NM_001368131.1:c.63-225_63-224del	NP_001355060.1:n.63-225_63-224del
NM_001368132.1:c.15-225_15-224del	NP_001355061.1:n.15-225_15-224del
NR_153398.2:n.292-8018_292-8017del