Canonical Allele Identifier: CA1225084628
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226894027G= , CM000663.2:g.226894027G= GRCh38
NC_000001.10:g.227081728G= , CM000663.1:g.227081728G= GRCh37
NC_000001.9:g.225148351G= NCBI36
NG_007381.1:g.28456G=
NG_012825.2:g.1492G=
NG_007381.2:g.28844G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.1093G= ENSP00000355741.2:p.Gly365=
ENST00000366782.6:c.1093G= ENSP00000355746.2:p.Gly365=
ENST00000366783.8:c.1093G= MANE Select ENSP00000355747.3:p.Gly365=
ENST00000471728.2:n.1731G=
ENST00000524196.6:c.1093G= ENSP00000429036.2:p.Gly365=
ENST00000626989.3:c.1093G= ENSP00000486498.2:p.Gly365=
ENST00000676467.1:c.*920G= ENSP00000504294.1:n.*920G=
ENST00000676747.1:c.1090G= ENSP00000503244.1:p.Gly364=
ENST00000676884.1:c.1093G= ENSP00000503200.1:p.Gly365=
ENST00000676888.1:c.*434G= ENSP00000504483.1:n.*434G=
ENST00000676907.1:c.*672G= ENSP00000504410.1:n.*672G=
ENST00000676945.1:c.1093G= ENSP00000504433.1:p.Gly365=
ENST00000677065.1:n.1654G=
ENST00000677414.1:c.1093G= ENSP00000503116.1:p.Gly365=
ENST00000677529.1:n.2823G=
ENST00000677596.1:c.*1315G= ENSP00000503618.1:n.*1315G=
ENST00000677599.1:c.1093G= ENSP00000503673.1:p.Gly365=
ENST00000677748.1:n.3348G=
ENST00000677880.1:c.658G= ENSP00000503121.1:p.Gly220=
ENST00000678021.1:c.*716G= ENSP00000504674.1:n.*716G=
ENST00000678233.1:c.1093G= ENSP00000504728.1:p.Gly365=
ENST00000678320.1:c.994G= ENSP00000503680.1:p.Gly332=
ENST00000678655.1:c.994G= ENSP00000504230.1:p.Gly332=
ENST00000678706.1:c.*470G= ENSP00000503659.1:n.*470G=
ENST00000678776.1:c.*1230G= ENSP00000504624.1:n.*1230G=
ENST00000678784.1:c.1072+2183G= ENSP00000504652.1:n.1072+2183G=
ENST00000678820.1:c.991G= ENSP00000504138.1:p.Gly331=
ENST00000678835.1:c.*756+2183G= ENSP00000504343.1:n.*756+2183G=
ENST00000679088.1:c.1093G= ENSP00000504727.1:p.Gly365=
ENST00000679098.1:c.1093G= ENSP00000504303.1:p.Gly365=
ENST00000366782.5:c.1192G= ENSP00000355746.1:p.Gly398=
ENST00000366783.7:c.1093G= ENSP00000355747.3:p.Gly365=
ENST00000422240.6:c.1090G= ENSP00000403737.2:p.Gly364=
ENST00000471728.1:n.351G=
ENST00000472139.2:c.661G= ENSP00000427806.1:p.Gly221=
ENST00000626989.2:c.1192G= ENSP00000486498.1:p.Gly398=
NM_000447.2:c.1093G= NP_000438.2:p.Gly365=
NM_012486.2:c.1090G= NP_036618.2:p.Gly364=
XM_005273199.2:c.1093G= XP_005273256.1:p.Gly365=
XM_011544236.1:c.661G= XP_011542538.1:p.Gly221=
XR_949149.1:n.1827G=
XM_005273199.4:c.1093G= XP_005273256.1:p.Gly365=
XM_017001835.1:c.1093G= XP_016857324.1:p.Gly365=
XM_017001836.1:c.1090G= XP_016857325.1:p.Gly364=
XR_001737316.2:n.1477+2183G=
XR_001737317.2:n.1477+2183G=
XR_001737318.2:n.1808G=
XR_001737319.1:n.2151G=
XR_001737320.1:n.2148G=
XR_001737321.1:n.1643G=
XR_949149.2:n.1805G=
XR_949150.3:n.2024G=
NM_000447.3:c.1093G= MANE Select NP_000438.2:p.Gly365=
NM_012486.3:c.1090G= NP_036618.2:p.Gly364=