Canonical Allele Identifier: CA2650788202

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226895383-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895383C>G , CM000663.2:g.226895383C>G	GRCh38
NC_000001.10:g.227083084C>G , CM000663.1:g.227083084C>G	GRCh37
NC_000001.9:g.225149707C>G	NCBI36
NG_007381.1:g.29812C>G
NG_012825.2:g.2848C>G
NG_007381.2:g.30200C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1192-41C>G	ENSP00000355741.2:n.1192-41C>G
ENST00000366782.6:c.1192-41C>G	ENSP00000355746.2:n.1192-41C>G
ENST00000366783.8:c.1192-41C>G MANE Select	ENSP00000355747.3:n.1192-41C>G
ENST00000471728.2:n.1830-41C>G
ENST00000524196.6:c.1192-41C>G	ENSP00000429036.2:n.1192-41C>G
ENST00000626989.3:c.1192-41C>G	ENSP00000486498.2:n.1192-41C>G
ENST00000676467.1:c.*1019-41C>G	ENSP00000504294.1:n.*1019-41C>G
ENST00000676747.1:c.1188+1258C>G	ENSP00000503244.1:n.1188+1258C>G
ENST00000676884.1:c.1192-41C>G	ENSP00000503200.1:n.1192-41C>G
ENST00000676888.1:c.*533-41C>G	ENSP00000504483.1:n.*533-41C>G
ENST00000676907.1:c.*771-41C>G	ENSP00000504410.1:n.*771-41C>G
ENST00000676945.1:c.1191+1258C>G	ENSP00000504433.1:n.1191+1258C>G
ENST00000677065.1:n.1753-41C>G
ENST00000677414.1:c.1192-41C>G	ENSP00000503116.1:n.1192-41C>G
ENST00000677529.1:n.2922-41C>G
ENST00000677596.1:c.*1414-41C>G	ENSP00000503618.1:n.*1414-41C>G
ENST00000677599.1:c.1191+1258C>G	ENSP00000503673.1:n.1191+1258C>G
ENST00000677748.1:n.3447-41C>G
ENST00000677880.1:c.757-41C>G	ENSP00000503121.1:n.757-41C>G
ENST00000678021.1:c.*815-41C>G	ENSP00000504674.1:n.*815-41C>G
ENST00000678233.1:c.1192-41C>G	ENSP00000504728.1:n.1192-41C>G
ENST00000678320.1:c.1093-41C>G	ENSP00000503680.1:n.1093-41C>G
ENST00000678655.1:c.1092+1258C>G	ENSP00000504230.1:n.1092+1258C>G
ENST00000678706.1:c.*569-41C>G	ENSP00000503659.1:n.*569-41C>G
ENST00000678776.1:c.*1329-41C>G	ENSP00000504624.1:n.*1329-41C>G
ENST00000678784.1:c.1073-2337C>G	ENSP00000504652.1:n.1073-2337C>G
ENST00000678820.1:c.1089+1258C>G	ENSP00000504138.1:n.1089+1258C>G
ENST00000678835.1:c.*757-2337C>G	ENSP00000504343.1:n.*757-2337C>G
ENST00000679088.1:c.1192-41C>G	ENSP00000504727.1:n.1192-41C>G
ENST00000679098.1:c.1192-41C>G	ENSP00000504303.1:n.1192-41C>G
ENST00000366782.5:c.1291-41C>G	ENSP00000355746.1:n.1291-41C>G
ENST00000366783.7:c.1192-41C>G	ENSP00000355747.3:n.1192-41C>G
ENST00000422240.6:c.1189-41C>G	ENSP00000403737.2:n.1189-41C>G
ENST00000471728.1:n.450-41C>G
ENST00000472139.2:c.760-41C>G	ENSP00000427806.1:n.760-41C>G
ENST00000626989.2:c.1291-41C>G	ENSP00000486498.1:n.1291-41C>G
NM_000447.2:c.1192-41C>G	NP_000438.2:n.1192-41C>G
NM_012486.2:c.1189-41C>G	NP_036618.2:n.1189-41C>G
XM_005273199.2:c.1192-41C>G	XP_005273256.1:n.1192-41C>G
XM_011544236.1:c.760-41C>G	XP_011542538.1:n.760-41C>G
XR_949149.1:n.1926-41C>G
XM_005273199.4:c.1192-41C>G	XP_005273256.1:n.1192-41C>G
XM_017001835.1:c.1192-41C>G	XP_016857324.1:n.1192-41C>G
XM_017001836.1:c.1189-41C>G	XP_016857325.1:n.1189-41C>G
XR_001737316.2:n.1478-2337C>G
XR_001737317.2:n.1478-2337C>G
XR_001737318.2:n.1907-41C>G
XR_001737319.1:n.2250-41C>G
XR_001737320.1:n.2247-41C>G
XR_001737321.1:n.1742-41C>G
XR_949149.2:n.1904-41C>G
XR_949150.3:n.2123-41C>G
NM_000447.3:c.1192-41C>G MANE Select	NP_000438.2:n.1192-41C>G
NM_012486.3:c.1189-41C>G	NP_036618.2:n.1189-41C>G