Canonical Allele Identifier: CA1225085489
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895963T= , CM000663.2:g.226895963T= GRCh38
NC_000001.10:g.227083664T= , CM000663.1:g.227083664T= GRCh37
NC_000001.9:g.225150287T= NCBI36
NG_007381.1:g.30392T=
NG_012825.2:g.3428T=
NG_007381.2:g.30780T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.*384T= ENSP00000355741.2:n.*384T=
ENST00000366782.6:c.*384T= ENSP00000355746.2:n.*384T=
ENST00000366783.8:c.*384T= MANE Select ENSP00000355747.3:n.*384T=
ENST00000471728.2:n.2369T=
ENST00000524196.6:c.*384T= ENSP00000429036.2:n.*384T=
ENST00000626989.3:c.*384T= ENSP00000486498.2:n.*384T=
ENST00000676467.1:c.*1558T= ENSP00000504294.1:n.*1558T=
ENST00000676747.1:c.1189-1757T= ENSP00000503244.1:n.1189-1757T=
ENST00000676884.1:c.*384T= ENSP00000503200.1:n.*384T=
ENST00000676888.1:c.*1072T= ENSP00000504483.1:n.*1072T=
ENST00000676907.1:c.*1310T= ENSP00000504410.1:n.*1310T=
ENST00000676945.1:c.1191+1838T= ENSP00000504433.1:n.1191+1838T=
ENST00000677065.1:n.2292T=
ENST00000677414.1:c.*384T= ENSP00000503116.1:n.*384T=
ENST00000677529.1:n.3461T=
ENST00000677596.1:c.*1953T= ENSP00000503618.1:n.*1953T=
ENST00000677599.1:c.1191+1838T= ENSP00000503673.1:n.1191+1838T=
ENST00000677748.1:n.3986T=
ENST00000677880.1:c.*384T= ENSP00000503121.1:n.*384T=
ENST00000678021.1:c.*1354T= ENSP00000504674.1:n.*1354T=
ENST00000678233.1:c.*8+376T= ENSP00000504728.1:n.*8+376T=
ENST00000678320.1:c.*384T= ENSP00000503680.1:n.*384T=
ENST00000678655.1:c.1093-1757T= ENSP00000504230.1:n.1093-1757T=
ENST00000678706.1:c.*1108T= ENSP00000503659.1:n.*1108T=
ENST00000678776.1:c.*1868T= ENSP00000504624.1:n.*1868T=
ENST00000678784.1:c.1073-1757T= ENSP00000504652.1:n.1073-1757T=
ENST00000678820.1:c.1090-1757T= ENSP00000504138.1:n.1090-1757T=
ENST00000678835.1:c.*757-1757T= ENSP00000504343.1:n.*757-1757T=
ENST00000679088.1:c.*384T= ENSP00000504727.1:n.*384T=
ENST00000679098.1:c.*8+376T= ENSP00000504303.1:n.*8+376T=
ENST00000366782.5:c.*384T= ENSP00000355746.1:n.*384T=
ENST00000366783.7:c.*384T= ENSP00000355747.3:n.*384T=
ENST00000626989.2:c.1830T= ENSP00000486498.1:n.1830T=
NM_000447.2:c.*384T= NP_000438.2:n.*384T=
NM_012486.2:c.*384T= NP_036618.2:n.*384T=
XM_005273199.2:c.*384T= XP_005273256.1:n.*384T=
XM_011544236.1:c.*384T= XP_011542538.1:n.*384T=
XM_005273199.4:c.*384T= XP_005273256.1:n.*384T=
XM_017001835.1:c.*384T= XP_016857324.1:n.*384T=
XM_017001836.1:c.*384T= XP_016857325.1:n.*384T=
XR_001737316.2:n.1478-1757T=
XR_001737317.2:n.1478-1757T=
XR_001737318.2:n.2446T=
XR_001737319.1:n.2789T=
XR_001737320.1:n.2786T=
XR_001737321.1:n.2281T=
XR_949149.2:n.2443T=
XR_949150.3:n.2662T=
NM_000447.3:c.*384T= MANE Select NP_000438.2:n.*384T=
NM_012486.3:c.*384T= NP_036618.2:n.*384T=