Canonical Allele Identifier: CA1225085304
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895537G= , CM000663.2:g.226895537G= GRCh38
NC_000001.10:g.227083238G= , CM000663.1:g.227083238G= GRCh37
NC_000001.9:g.225149861G= NCBI36
NG_007381.1:g.29966G=
NG_012825.2:g.3002G=
NG_007381.2:g.30354G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.1305G= ENSP00000355741.2:p.Arg435=
ENST00000366782.6:c.1305G= ENSP00000355746.2:p.Arg435=
ENST00000366783.8:c.1305G= MANE Select ENSP00000355747.3:p.Arg435=
ENST00000471728.2:n.1943G=
ENST00000524196.6:c.1305G= ENSP00000429036.2:p.Arg435=
ENST00000626989.3:c.1305G= ENSP00000486498.2:p.Arg435=
ENST00000676467.1:c.*1132G= ENSP00000504294.1:n.*1132G=
ENST00000676747.1:c.1188+1412G= ENSP00000503244.1:n.1188+1412G=
ENST00000676884.1:c.1305G= ENSP00000503200.1:p.Arg435=
ENST00000676888.1:c.*646G= ENSP00000504483.1:n.*646G=
ENST00000676907.1:c.*884G= ENSP00000504410.1:n.*884G=
ENST00000676945.1:c.1191+1412G= ENSP00000504433.1:n.1191+1412G=
ENST00000677065.1:n.1866G=
ENST00000677414.1:c.1305G= ENSP00000503116.1:p.Arg435=
ENST00000677529.1:n.3035G=
ENST00000677596.1:c.*1527G= ENSP00000503618.1:n.*1527G=
ENST00000677599.1:c.1191+1412G= ENSP00000503673.1:n.1191+1412G=
ENST00000677748.1:n.3560G=
ENST00000677880.1:c.870G= ENSP00000503121.1:p.Arg290=
ENST00000678021.1:c.*928G= ENSP00000504674.1:n.*928G=
ENST00000678233.1:c.1305G= ENSP00000504728.1:p.Arg435=
ENST00000678320.1:c.1206G= ENSP00000503680.1:p.Arg402=
ENST00000678655.1:c.1092+1412G= ENSP00000504230.1:n.1092+1412G=
ENST00000678706.1:c.*682G= ENSP00000503659.1:n.*682G=
ENST00000678776.1:c.*1442G= ENSP00000504624.1:n.*1442G=
ENST00000678784.1:c.1073-2183G= ENSP00000504652.1:n.1073-2183G=
ENST00000678820.1:c.1089+1412G= ENSP00000504138.1:n.1089+1412G=
ENST00000678835.1:c.*757-2183G= ENSP00000504343.1:n.*757-2183G=
ENST00000679088.1:c.1305G= ENSP00000504727.1:p.Arg435=
ENST00000679098.1:c.1305G= ENSP00000504303.1:p.Arg435=
ENST00000366782.5:c.1404G= ENSP00000355746.1:p.Arg468=
ENST00000366783.7:c.1305G= ENSP00000355747.3:p.Arg435=
ENST00000422240.6:c.1302G= ENSP00000403737.2:p.Arg434=
ENST00000471728.1:n.563G=
ENST00000472139.2:c.873G= ENSP00000427806.1:p.Arg291=
ENST00000626989.2:c.1404G= ENSP00000486498.1:p.Arg468=
NM_000447.2:c.1305G= NP_000438.2:p.Arg435=
NM_012486.2:c.1302G= NP_036618.2:p.Arg434=
XM_005273199.2:c.1305G= XP_005273256.1:p.Arg435=
XM_011544236.1:c.873G= XP_011542538.1:p.Arg291=
XR_949149.1:n.2039G=
XM_005273199.4:c.1305G= XP_005273256.1:p.Arg435=
XM_017001835.1:c.1305G= XP_016857324.1:p.Arg435=
XM_017001836.1:c.1302G= XP_016857325.1:p.Arg434=
XR_001737316.2:n.1478-2183G=
XR_001737317.2:n.1478-2183G=
XR_001737318.2:n.2020G=
XR_001737319.1:n.2363G=
XR_001737320.1:n.2360G=
XR_001737321.1:n.1855G=
XR_949149.2:n.2017G=
XR_949150.3:n.2236G=
NM_000447.3:c.1305G= MANE Select NP_000438.2:p.Arg435=
NM_012486.3:c.1302G= NP_036618.2:p.Arg434=