Canonical Allele Identifier: CA1225085360
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895671A= , CM000663.2:g.226895671A= GRCh38
NC_000001.10:g.227083372A= , CM000663.1:g.227083372A= GRCh37
NC_000001.9:g.225149995A= NCBI36
NG_007381.1:g.30100A=
NG_012825.2:g.3136A=
NG_007381.2:g.30488A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.*92A= ENSP00000355741.2:n.*92A=
ENST00000366782.6:c.*92A= ENSP00000355746.2:n.*92A=
ENST00000366783.8:c.*92A= MANE Select ENSP00000355747.3:n.*92A=
ENST00000471728.2:n.2077A=
ENST00000524196.6:c.*92A= ENSP00000429036.2:n.*92A=
ENST00000626989.3:c.*92A= ENSP00000486498.2:n.*92A=
ENST00000676467.1:c.*1266A= ENSP00000504294.1:n.*1266A=
ENST00000676747.1:c.1188+1546A= ENSP00000503244.1:n.1188+1546A=
ENST00000676884.1:c.*92A= ENSP00000503200.1:n.*92A=
ENST00000676888.1:c.*780A= ENSP00000504483.1:n.*780A=
ENST00000676907.1:c.*1018A= ENSP00000504410.1:n.*1018A=
ENST00000676945.1:c.1191+1546A= ENSP00000504433.1:n.1191+1546A=
ENST00000677065.1:n.2000A=
ENST00000677414.1:c.*92A= ENSP00000503116.1:n.*92A=
ENST00000677529.1:n.3169A=
ENST00000677596.1:c.*1661A= ENSP00000503618.1:n.*1661A=
ENST00000677599.1:c.1191+1546A= ENSP00000503673.1:n.1191+1546A=
ENST00000677748.1:n.3694A=
ENST00000677880.1:c.*92A= ENSP00000503121.1:n.*92A=
ENST00000678021.1:c.*1062A= ENSP00000504674.1:n.*1062A=
ENST00000678233.1:c.*8+84A= ENSP00000504728.1:n.*8+84A=
ENST00000678320.1:c.*92A= ENSP00000503680.1:n.*92A=
ENST00000678655.1:c.1092+1546A= ENSP00000504230.1:n.1092+1546A=
ENST00000678706.1:c.*816A= ENSP00000503659.1:n.*816A=
ENST00000678776.1:c.*1576A= ENSP00000504624.1:n.*1576A=
ENST00000678784.1:c.1073-2049A= ENSP00000504652.1:n.1073-2049A=
ENST00000678820.1:c.1089+1546A= ENSP00000504138.1:n.1089+1546A=
ENST00000678835.1:c.*757-2049A= ENSP00000504343.1:n.*757-2049A=
ENST00000679088.1:c.*92A= ENSP00000504727.1:n.*92A=
ENST00000679098.1:c.*8+84A= ENSP00000504303.1:n.*8+84A=
ENST00000366782.5:c.*92A= ENSP00000355746.1:n.*92A=
ENST00000366783.7:c.*92A= ENSP00000355747.3:n.*92A=
ENST00000422240.6:c.*92A= ENSP00000403737.2:n.*92A=
ENST00000472139.2:c.*92A= ENSP00000427806.1:n.*92A=
ENST00000626989.2:c.1538A= ENSP00000486498.1:n.1538A=
NM_000447.2:c.*92A= NP_000438.2:n.*92A=
NM_012486.2:c.*92A= NP_036618.2:n.*92A=
XM_005273199.2:c.*92A= XP_005273256.1:n.*92A=
XM_011544236.1:c.*92A= XP_011542538.1:n.*92A=
XM_005273199.4:c.*92A= XP_005273256.1:n.*92A=
XM_017001835.1:c.*92A= XP_016857324.1:n.*92A=
XM_017001836.1:c.*92A= XP_016857325.1:n.*92A=
XR_001737316.2:n.1478-2049A=
XR_001737317.2:n.1478-2049A=
XR_001737318.2:n.2154A=
XR_001737319.1:n.2497A=
XR_001737320.1:n.2494A=
XR_001737321.1:n.1989A=
XR_949149.2:n.2151A=
XR_949150.3:n.2370A=
NM_000447.3:c.*92A= MANE Select NP_000438.2:n.*92A=
NM_012486.3:c.*92A= NP_036618.2:n.*92A=