Canonical Allele Identifier: CA1143064714
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226893862C= , CM000663.2:g.226893862C= GRCh38
NC_000001.10:g.227081563C= , CM000663.1:g.227081563C= GRCh37
NC_000001.9:g.225148186C= NCBI36
NG_007381.1:g.28291C=
NG_012825.2:g.1327C=
NG_007381.2:g.28679C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.1073-145C= ENSP00000355741.2:n.1073-145C=
ENST00000366782.6:c.1073-145C= ENSP00000355746.2:n.1073-145C=
ENST00000366783.8:c.1073-145C= MANE Select ENSP00000355747.3:n.1073-145C=
ENST00000471728.2:n.1711-145C=
ENST00000524196.6:c.1073-145C= ENSP00000429036.2:n.1073-145C=
ENST00000626989.3:c.1073-145C= ENSP00000486498.2:n.1073-145C=
ENST00000676467.1:c.*900-145C= ENSP00000504294.1:n.*900-145C=
ENST00000676747.1:c.1070-145C= ENSP00000503244.1:n.1070-145C=
ENST00000676884.1:c.1073-145C= ENSP00000503200.1:n.1073-145C=
ENST00000676888.1:c.*414-145C= ENSP00000504483.1:n.*414-145C=
ENST00000676907.1:c.*652-145C= ENSP00000504410.1:n.*652-145C=
ENST00000676945.1:c.1073-145C= ENSP00000504433.1:n.1073-145C=
ENST00000677065.1:n.1634-145C=
ENST00000677414.1:c.1073-145C= ENSP00000503116.1:n.1073-145C=
ENST00000677529.1:n.2803-145C=
ENST00000677596.1:c.*1295-145C= ENSP00000503618.1:n.*1295-145C=
ENST00000677599.1:c.1073-145C= ENSP00000503673.1:n.1073-145C=
ENST00000677748.1:n.3328-145C=
ENST00000677880.1:c.638-145C= ENSP00000503121.1:n.638-145C=
ENST00000678021.1:c.*696-145C= ENSP00000504674.1:n.*696-145C=
ENST00000678233.1:c.1073-145C= ENSP00000504728.1:n.1073-145C=
ENST00000678320.1:c.974-145C= ENSP00000503680.1:n.974-145C=
ENST00000678655.1:c.974-145C= ENSP00000504230.1:n.974-145C=
ENST00000678706.1:c.*450-145C= ENSP00000503659.1:n.*450-145C=
ENST00000678776.1:c.*1210-145C= ENSP00000504624.1:n.*1210-145C=
ENST00000678784.1:c.1072+2018C= ENSP00000504652.1:n.1072+2018C=
ENST00000678820.1:c.971-145C= ENSP00000504138.1:n.971-145C=
ENST00000678835.1:c.*756+2018C= ENSP00000504343.1:n.*756+2018C=
ENST00000679088.1:c.1073-145C= ENSP00000504727.1:n.1073-145C=
ENST00000679098.1:c.1073-145C= ENSP00000504303.1:n.1073-145C=
ENST00000366782.5:c.1172-145C= ENSP00000355746.1:n.1172-145C=
ENST00000366783.7:c.1073-145C= ENSP00000355747.3:n.1073-145C=
ENST00000422240.6:c.1070-145C= ENSP00000403737.2:n.1070-145C=
ENST00000471728.1:n.331-145C=
ENST00000472139.2:c.641-145C= ENSP00000427806.1:n.641-145C=
ENST00000626989.2:c.1172-145C= ENSP00000486498.1:n.1172-145C=
NM_000447.2:c.1073-145C= NP_000438.2:n.1073-145C=
NM_012486.2:c.1070-145C= NP_036618.2:n.1070-145C=
XM_005273199.2:c.1073-145C= XP_005273256.1:n.1073-145C=
XM_011544236.1:c.641-145C= XP_011542538.1:n.641-145C=
XR_949149.1:n.1807-145C=
XM_005273199.4:c.1073-145C= XP_005273256.1:n.1073-145C=
XM_017001835.1:c.1073-145C= XP_016857324.1:n.1073-145C=
XM_017001836.1:c.1070-145C= XP_016857325.1:n.1070-145C=
XR_001737316.2:n.1477+2018C=
XR_001737317.2:n.1477+2018C=
XR_001737318.2:n.1788-145C=
XR_001737319.1:n.2131-145C=
XR_001737320.1:n.2128-145C=
XR_001737321.1:n.1623-145C=
XR_949149.2:n.1785-145C=
XR_949150.3:n.2004-145C=
NM_000447.3:c.1073-145C= MANE Select NP_000438.2:n.1073-145C=
NM_012486.3:c.1070-145C= NP_036618.2:n.1070-145C=