Canonical Allele Identifier: CA1225084634
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226894041C= , CM000663.2:g.226894041C= GRCh38
NC_000001.10:g.227081742C= , CM000663.1:g.227081742C= GRCh37
NC_000001.9:g.225148365C= NCBI36
NG_007381.1:g.28470C=
NG_012825.2:g.1506C=
NG_007381.2:g.28858C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.1107C= ENSP00000355741.2:p.Phe369=
ENST00000366782.6:c.1107C= ENSP00000355746.2:p.Phe369=
ENST00000366783.8:c.1107C= MANE Select ENSP00000355747.3:p.Phe369=
ENST00000471728.2:n.1745C=
ENST00000524196.6:c.1107C= ENSP00000429036.2:p.Phe369=
ENST00000626989.3:c.1107C= ENSP00000486498.2:p.Phe369=
ENST00000676467.1:c.*934C= ENSP00000504294.1:n.*934C=
ENST00000676747.1:c.1104C= ENSP00000503244.1:p.Phe368=
ENST00000676884.1:c.1107C= ENSP00000503200.1:p.Phe369=
ENST00000676888.1:c.*448C= ENSP00000504483.1:n.*448C=
ENST00000676907.1:c.*686C= ENSP00000504410.1:n.*686C=
ENST00000676945.1:c.1107C= ENSP00000504433.1:p.Phe369=
ENST00000677065.1:n.1668C=
ENST00000677414.1:c.1107C= ENSP00000503116.1:p.Phe369=
ENST00000677529.1:n.2837C=
ENST00000677596.1:c.*1329C= ENSP00000503618.1:n.*1329C=
ENST00000677599.1:c.1107C= ENSP00000503673.1:p.Phe369=
ENST00000677748.1:n.3362C=
ENST00000677880.1:c.672C= ENSP00000503121.1:p.Phe224=
ENST00000678021.1:c.*730C= ENSP00000504674.1:n.*730C=
ENST00000678233.1:c.1107C= ENSP00000504728.1:p.Phe369=
ENST00000678320.1:c.1008C= ENSP00000503680.1:p.Phe336=
ENST00000678655.1:c.1008C= ENSP00000504230.1:p.Phe336=
ENST00000678706.1:c.*484C= ENSP00000503659.1:n.*484C=
ENST00000678776.1:c.*1244C= ENSP00000504624.1:n.*1244C=
ENST00000678784.1:c.1072+2197C= ENSP00000504652.1:n.1072+2197C=
ENST00000678820.1:c.1005C= ENSP00000504138.1:p.Phe335=
ENST00000678835.1:c.*756+2197C= ENSP00000504343.1:n.*756+2197C=
ENST00000679088.1:c.1107C= ENSP00000504727.1:p.Phe369=
ENST00000679098.1:c.1107C= ENSP00000504303.1:p.Phe369=
ENST00000366782.5:c.1206C= ENSP00000355746.1:p.Phe402=
ENST00000366783.7:c.1107C= ENSP00000355747.3:p.Phe369=
ENST00000422240.6:c.1104C= ENSP00000403737.2:p.Phe368=
ENST00000471728.1:n.365C=
ENST00000472139.2:c.675C= ENSP00000427806.1:p.Phe225=
ENST00000626989.2:c.1206C= ENSP00000486498.1:p.Phe402=
NM_000447.2:c.1107C= NP_000438.2:p.Phe369=
NM_012486.2:c.1104C= NP_036618.2:p.Phe368=
XM_005273199.2:c.1107C= XP_005273256.1:p.Phe369=
XM_011544236.1:c.675C= XP_011542538.1:p.Phe225=
XR_949149.1:n.1841C=
XM_005273199.4:c.1107C= XP_005273256.1:p.Phe369=
XM_017001835.1:c.1107C= XP_016857324.1:p.Phe369=
XM_017001836.1:c.1104C= XP_016857325.1:p.Phe368=
XR_001737316.2:n.1477+2197C=
XR_001737317.2:n.1477+2197C=
XR_001737318.2:n.1822C=
XR_001737319.1:n.2165C=
XR_001737320.1:n.2162C=
XR_001737321.1:n.1657C=
XR_949149.2:n.1819C=
XR_949150.3:n.2038C=
NM_000447.3:c.1107C= MANE Select NP_000438.2:p.Phe369=
NM_012486.3:c.1104C= NP_036618.2:p.Phe368=