Canonical Allele Identifier: CA1143486363
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895795C= , CM000663.2:g.226895795C= GRCh38
NC_000001.10:g.227083496C= , CM000663.1:g.227083496C= GRCh37
NC_000001.9:g.225150119C= NCBI36
NG_007381.1:g.30224C=
NG_012825.2:g.3260C=
NG_007381.2:g.30612C=

Transcript Alleles

HGVS Amino-acid change
ENST00000366779.6:c.*216C= ENSP00000355741.2:n.*216C=
ENST00000366782.6:c.*216C= ENSP00000355746.2:n.*216C=
ENST00000366783.8:c.*216C= MANE Select ENSP00000355747.3:n.*216C=
ENST00000471728.2:n.2201C=
ENST00000524196.6:c.*216C= ENSP00000429036.2:n.*216C=
ENST00000626989.3:c.*216C= ENSP00000486498.2:n.*216C=
ENST00000676467.1:c.*1390C= ENSP00000504294.1:n.*1390C=
ENST00000676747.1:c.1188+1670C= ENSP00000503244.1:n.1188+1670C=
ENST00000676884.1:c.*216C= ENSP00000503200.1:n.*216C=
ENST00000676888.1:c.*904C= ENSP00000504483.1:n.*904C=
ENST00000676907.1:c.*1142C= ENSP00000504410.1:n.*1142C=
ENST00000676945.1:c.1191+1670C= ENSP00000504433.1:n.1191+1670C=
ENST00000677065.1:n.2124C=
ENST00000677414.1:c.*216C= ENSP00000503116.1:n.*216C=
ENST00000677529.1:n.3293C=
ENST00000677596.1:c.*1785C= ENSP00000503618.1:n.*1785C=
ENST00000677599.1:c.1191+1670C= ENSP00000503673.1:n.1191+1670C=
ENST00000677748.1:n.3818C=
ENST00000677880.1:c.*216C= ENSP00000503121.1:n.*216C=
ENST00000678021.1:c.*1186C= ENSP00000504674.1:n.*1186C=
ENST00000678233.1:c.*8+208C= ENSP00000504728.1:n.*8+208C=
ENST00000678320.1:c.*216C= ENSP00000503680.1:n.*216C=
ENST00000678655.1:c.1092+1670C= ENSP00000504230.1:n.1092+1670C=
ENST00000678706.1:c.*940C= ENSP00000503659.1:n.*940C=
ENST00000678776.1:c.*1700C= ENSP00000504624.1:n.*1700C=
ENST00000678784.1:c.1073-1925C= ENSP00000504652.1:n.1073-1925C=
ENST00000678820.1:c.1089+1670C= ENSP00000504138.1:n.1089+1670C=
ENST00000678835.1:c.*757-1925C= ENSP00000504343.1:n.*757-1925C=
ENST00000679088.1:c.*216C= ENSP00000504727.1:n.*216C=
ENST00000679098.1:c.*8+208C= ENSP00000504303.1:n.*8+208C=
ENST00000366782.5:c.*216C= ENSP00000355746.1:n.*216C=
ENST00000366783.7:c.*216C= ENSP00000355747.3:n.*216C=
ENST00000422240.6:c.*216C= ENSP00000403737.2:n.*216C=
ENST00000626989.2:c.1662C= ENSP00000486498.1:n.1662C=
NM_000447.2:c.*216C= NP_000438.2:n.*216C=
NM_012486.2:c.*216C= NP_036618.2:n.*216C=
XM_005273199.2:c.*216C= XP_005273256.1:n.*216C=
XM_011544236.1:c.*216C= XP_011542538.1:n.*216C=
XM_005273199.4:c.*216C= XP_005273256.1:n.*216C=
XM_017001835.1:c.*216C= XP_016857324.1:n.*216C=
XM_017001836.1:c.*216C= XP_016857325.1:n.*216C=
XR_001737316.2:n.1478-1925C=
XR_001737317.2:n.1478-1925C=
XR_001737318.2:n.2278C=
XR_001737319.1:n.2621C=
XR_001737320.1:n.2618C=
XR_001737321.1:n.2113C=
XR_949149.2:n.2275C=
XR_949150.3:n.2494C=
NM_000447.3:c.*216C= MANE Select NP_000438.2:n.*216C=
NM_012486.3:c.*216C= NP_036618.2:n.*216C=