Canonical Allele Identifier: CA1225085311
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895560C= , CM000663.2:g.226895560C= GRCh38
NC_000001.10:g.227083261C= , CM000663.1:g.227083261C= GRCh37
NC_000001.9:g.225149884C= NCBI36
NG_007381.1:g.29989C=
NG_012825.2:g.3025C=
NG_007381.2:g.30377C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.1328C= ENSP00000355741.2:p.Ser443=
ENST00000366782.6:c.1328C= ENSP00000355746.2:p.Ser443=
ENST00000366783.8:c.1328C= MANE Select ENSP00000355747.3:p.Ser443=
ENST00000471728.2:n.1966C=
ENST00000524196.6:c.1328C= ENSP00000429036.2:p.Ser443=
ENST00000626989.3:c.1328C= ENSP00000486498.2:p.Ser443=
ENST00000676467.1:c.*1155C= ENSP00000504294.1:n.*1155C=
ENST00000676747.1:c.1188+1435C= ENSP00000503244.1:n.1188+1435C=
ENST00000676884.1:c.1328C= ENSP00000503200.1:p.Ser443=
ENST00000676888.1:c.*669C= ENSP00000504483.1:n.*669C=
ENST00000676907.1:c.*907C= ENSP00000504410.1:n.*907C=
ENST00000676945.1:c.1191+1435C= ENSP00000504433.1:n.1191+1435C=
ENST00000677065.1:n.1889C=
ENST00000677414.1:c.1328C= ENSP00000503116.1:p.Ser443=
ENST00000677529.1:n.3058C=
ENST00000677596.1:c.*1550C= ENSP00000503618.1:n.*1550C=
ENST00000677599.1:c.1191+1435C= ENSP00000503673.1:n.1191+1435C=
ENST00000677748.1:n.3583C=
ENST00000677880.1:c.893C= ENSP00000503121.1:p.Ser298=
ENST00000678021.1:c.*951C= ENSP00000504674.1:n.*951C=
ENST00000678233.1:c.1328C= ENSP00000504728.1:p.Ser443=
ENST00000678320.1:c.1229C= ENSP00000503680.1:p.Ser410=
ENST00000678655.1:c.1092+1435C= ENSP00000504230.1:n.1092+1435C=
ENST00000678706.1:c.*705C= ENSP00000503659.1:n.*705C=
ENST00000678776.1:c.*1465C= ENSP00000504624.1:n.*1465C=
ENST00000678784.1:c.1073-2160C= ENSP00000504652.1:n.1073-2160C=
ENST00000678820.1:c.1089+1435C= ENSP00000504138.1:n.1089+1435C=
ENST00000678835.1:c.*757-2160C= ENSP00000504343.1:n.*757-2160C=
ENST00000679088.1:c.1328C= ENSP00000504727.1:p.Ser443=
ENST00000679098.1:c.1328C= ENSP00000504303.1:p.Ser443=
ENST00000366782.5:c.1427C= ENSP00000355746.1:p.Ser476=
ENST00000366783.7:c.1328C= ENSP00000355747.3:p.Ser443=
ENST00000422240.6:c.1325C= ENSP00000403737.2:p.Ser442=
ENST00000472139.2:c.896C= ENSP00000427806.1:p.Ser299=
ENST00000626989.2:c.1427C= ENSP00000486498.1:p.Ser476=
NM_000447.2:c.1328C= NP_000438.2:p.Ser443=
NM_012486.2:c.1325C= NP_036618.2:p.Ser442=
XM_005273199.2:c.1328C= XP_005273256.1:p.Ser443=
XM_011544236.1:c.896C= XP_011542538.1:p.Ser299=
XM_005273199.4:c.1328C= XP_005273256.1:p.Ser443=
XM_017001835.1:c.1328C= XP_016857324.1:p.Ser443=
XM_017001836.1:c.1325C= XP_016857325.1:p.Ser442=
XR_001737316.2:n.1478-2160C=
XR_001737317.2:n.1478-2160C=
XR_001737318.2:n.2043C=
XR_001737319.1:n.2386C=
XR_001737320.1:n.2383C=
XR_001737321.1:n.1878C=
XR_949149.2:n.2040C=
XR_949150.3:n.2259C=
NM_000447.3:c.1328C= MANE Select NP_000438.2:p.Ser443=
NM_012486.3:c.1325C= NP_036618.2:p.Ser442=