Canonical Allele Identifier: CA1143493950
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226896020T= , CM000663.2:g.226896020T= GRCh38
NC_000001.10:g.227083721T= , CM000663.1:g.227083721T= GRCh37
NC_000001.9:g.225150344T= NCBI36
NG_007381.1:g.30449T=
NG_012825.2:g.3485T=
NG_007381.2:g.30837T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.*441T= ENSP00000355741.2:n.*441T=
ENST00000366782.6:c.*441T= ENSP00000355746.2:n.*441T=
ENST00000366783.8:c.*441T= MANE Select ENSP00000355747.3:n.*441T=
ENST00000471728.2:n.2426T=
ENST00000524196.6:c.*441T= ENSP00000429036.2:n.*441T=
ENST00000626989.3:c.*441T= ENSP00000486498.2:n.*441T=
ENST00000676467.1:c.*1615T= ENSP00000504294.1:n.*1615T=
ENST00000676747.1:c.1189-1700T= ENSP00000503244.1:n.1189-1700T=
ENST00000676884.1:c.*441T= ENSP00000503200.1:n.*441T=
ENST00000676888.1:c.*1129T= ENSP00000504483.1:n.*1129T=
ENST00000676907.1:c.*1367T= ENSP00000504410.1:n.*1367T=
ENST00000676945.1:c.1191+1895T= ENSP00000504433.1:n.1191+1895T=
ENST00000677065.1:n.2349T=
ENST00000677414.1:c.*441T= ENSP00000503116.1:n.*441T=
ENST00000677529.1:n.3518T=
ENST00000677596.1:c.*2010T= ENSP00000503618.1:n.*2010T=
ENST00000677599.1:c.1191+1895T= ENSP00000503673.1:n.1191+1895T=
ENST00000677748.1:n.4043T=
ENST00000677880.1:c.*441T= ENSP00000503121.1:n.*441T=
ENST00000678021.1:c.*1411T= ENSP00000504674.1:n.*1411T=
ENST00000678233.1:c.*8+433T= ENSP00000504728.1:n.*8+433T=
ENST00000678320.1:c.*441T= ENSP00000503680.1:n.*441T=
ENST00000678655.1:c.1093-1700T= ENSP00000504230.1:n.1093-1700T=
ENST00000678706.1:c.*1165T= ENSP00000503659.1:n.*1165T=
ENST00000678776.1:c.*1925T= ENSP00000504624.1:n.*1925T=
ENST00000678784.1:c.1073-1700T= ENSP00000504652.1:n.1073-1700T=
ENST00000678820.1:c.1090-1700T= ENSP00000504138.1:n.1090-1700T=
ENST00000678835.1:c.*757-1700T= ENSP00000504343.1:n.*757-1700T=
ENST00000679088.1:c.*441T= ENSP00000504727.1:n.*441T=
ENST00000679098.1:c.*8+433T= ENSP00000504303.1:n.*8+433T=
ENST00000366782.5:c.*441T= ENSP00000355746.1:n.*441T=
ENST00000366783.7:c.*441T= ENSP00000355747.3:n.*441T=
ENST00000626989.2:c.1887T= ENSP00000486498.1:n.1887T=
NM_000447.2:c.*441T= NP_000438.2:n.*441T=
NM_012486.2:c.*441T= NP_036618.2:n.*441T=
XM_005273199.2:c.*441T= XP_005273256.1:n.*441T=
XM_011544236.1:c.*441T= XP_011542538.1:n.*441T=
XM_005273199.4:c.*441T= XP_005273256.1:n.*441T=
XM_017001835.1:c.*441T= XP_016857324.1:n.*441T=
XM_017001836.1:c.*441T= XP_016857325.1:n.*441T=
XR_001737316.2:n.1478-1700T=
XR_001737317.2:n.1478-1700T=
XR_001737318.2:n.2503T=
XR_001737319.1:n.2846T=
XR_001737320.1:n.2843T=
XR_001737321.1:n.2338T=
XR_949149.2:n.2500T=
XR_949150.3:n.2719T=
NM_000447.3:c.*441T= MANE Select NP_000438.2:n.*441T=
NM_012486.3:c.*441T= NP_036618.2:n.*441T=