Canonical Allele Identifier: CA1225084647
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226894080C= , CM000663.2:g.226894080C= GRCh38
NC_000001.10:g.227081781C= , CM000663.1:g.227081781C= GRCh37
NC_000001.9:g.225148404C= NCBI36
NG_007381.1:g.28509C=
NG_012825.2:g.1545C=
NG_007381.2:g.28897C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.1146C= ENSP00000355741.2:p.Ser382=
ENST00000366782.6:c.1146C= ENSP00000355746.2:p.Ser382=
ENST00000366783.8:c.1146C= MANE Select ENSP00000355747.3:p.Ser382=
ENST00000471728.2:n.1784C=
ENST00000524196.6:c.1146C= ENSP00000429036.2:p.Ser382=
ENST00000626989.3:c.1146C= ENSP00000486498.2:p.Ser382=
ENST00000676467.1:c.*973C= ENSP00000504294.1:n.*973C=
ENST00000676747.1:c.1143C= ENSP00000503244.1:p.Ser381=
ENST00000676884.1:c.1146C= ENSP00000503200.1:p.Ser382=
ENST00000676888.1:c.*487C= ENSP00000504483.1:n.*487C=
ENST00000676907.1:c.*725C= ENSP00000504410.1:n.*725C=
ENST00000676945.1:c.1146C= ENSP00000504433.1:p.Ser382=
ENST00000677065.1:n.1707C=
ENST00000677414.1:c.1146C= ENSP00000503116.1:p.Ser382=
ENST00000677529.1:n.2876C=
ENST00000677596.1:c.*1368C= ENSP00000503618.1:n.*1368C=
ENST00000677599.1:c.1146C= ENSP00000503673.1:p.Ser382=
ENST00000677748.1:n.3401C=
ENST00000677880.1:c.711C= ENSP00000503121.1:p.Ser237=
ENST00000678021.1:c.*769C= ENSP00000504674.1:n.*769C=
ENST00000678233.1:c.1146C= ENSP00000504728.1:p.Ser382=
ENST00000678320.1:c.1047C= ENSP00000503680.1:p.Ser349=
ENST00000678655.1:c.1047C= ENSP00000504230.1:p.Ser349=
ENST00000678706.1:c.*523C= ENSP00000503659.1:n.*523C=
ENST00000678776.1:c.*1283C= ENSP00000504624.1:n.*1283C=
ENST00000678784.1:c.1072+2236C= ENSP00000504652.1:n.1072+2236C=
ENST00000678820.1:c.1044C= ENSP00000504138.1:p.Ser348=
ENST00000678835.1:c.*756+2236C= ENSP00000504343.1:n.*756+2236C=
ENST00000679088.1:c.1146C= ENSP00000504727.1:p.Ser382=
ENST00000679098.1:c.1146C= ENSP00000504303.1:p.Ser382=
ENST00000366782.5:c.1245C= ENSP00000355746.1:p.Ser415=
ENST00000366783.7:c.1146C= ENSP00000355747.3:p.Ser382=
ENST00000422240.6:c.1143C= ENSP00000403737.2:p.Ser381=
ENST00000471728.1:n.404C=
ENST00000472139.2:c.714C= ENSP00000427806.1:p.Ser238=
ENST00000626989.2:c.1245C= ENSP00000486498.1:p.Ser415=
NM_000447.2:c.1146C= NP_000438.2:p.Ser382=
NM_012486.2:c.1143C= NP_036618.2:p.Ser381=
XM_005273199.2:c.1146C= XP_005273256.1:p.Ser382=
XM_011544236.1:c.714C= XP_011542538.1:p.Ser238=
XR_949149.1:n.1880C=
XM_005273199.4:c.1146C= XP_005273256.1:p.Ser382=
XM_017001835.1:c.1146C= XP_016857324.1:p.Ser382=
XM_017001836.1:c.1143C= XP_016857325.1:p.Ser381=
XR_001737316.2:n.1477+2236C=
XR_001737317.2:n.1477+2236C=
XR_001737318.2:n.1861C=
XR_001737319.1:n.2204C=
XR_001737320.1:n.2201C=
XR_001737321.1:n.1696C=
XR_949149.2:n.1858C=
XR_949150.3:n.2077C=
NM_000447.3:c.1146C= MANE Select NP_000438.2:p.Ser382=
NM_012486.3:c.1143C= NP_036618.2:p.Ser381=