Canonical Allele Identifier: CA1225085499
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895997T= , CM000663.2:g.226895997T= GRCh38
NC_000001.10:g.227083698T= , CM000663.1:g.227083698T= GRCh37
NC_000001.9:g.225150321T= NCBI36
NG_007381.1:g.30426T=
NG_012825.2:g.3462T=
NG_007381.2:g.30814T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.*418T= ENSP00000355741.2:n.*418T=
ENST00000366782.6:c.*418T= ENSP00000355746.2:n.*418T=
ENST00000366783.8:c.*418T= MANE Select ENSP00000355747.3:n.*418T=
ENST00000471728.2:n.2403T=
ENST00000524196.6:c.*418T= ENSP00000429036.2:n.*418T=
ENST00000626989.3:c.*418T= ENSP00000486498.2:n.*418T=
ENST00000676467.1:c.*1592T= ENSP00000504294.1:n.*1592T=
ENST00000676747.1:c.1189-1723T= ENSP00000503244.1:n.1189-1723T=
ENST00000676884.1:c.*418T= ENSP00000503200.1:n.*418T=
ENST00000676888.1:c.*1106T= ENSP00000504483.1:n.*1106T=
ENST00000676907.1:c.*1344T= ENSP00000504410.1:n.*1344T=
ENST00000676945.1:c.1191+1872T= ENSP00000504433.1:n.1191+1872T=
ENST00000677065.1:n.2326T=
ENST00000677414.1:c.*418T= ENSP00000503116.1:n.*418T=
ENST00000677529.1:n.3495T=
ENST00000677596.1:c.*1987T= ENSP00000503618.1:n.*1987T=
ENST00000677599.1:c.1191+1872T= ENSP00000503673.1:n.1191+1872T=
ENST00000677748.1:n.4020T=
ENST00000677880.1:c.*418T= ENSP00000503121.1:n.*418T=
ENST00000678021.1:c.*1388T= ENSP00000504674.1:n.*1388T=
ENST00000678233.1:c.*8+410T= ENSP00000504728.1:n.*8+410T=
ENST00000678320.1:c.*418T= ENSP00000503680.1:n.*418T=
ENST00000678655.1:c.1093-1723T= ENSP00000504230.1:n.1093-1723T=
ENST00000678706.1:c.*1142T= ENSP00000503659.1:n.*1142T=
ENST00000678776.1:c.*1902T= ENSP00000504624.1:n.*1902T=
ENST00000678784.1:c.1073-1723T= ENSP00000504652.1:n.1073-1723T=
ENST00000678820.1:c.1090-1723T= ENSP00000504138.1:n.1090-1723T=
ENST00000678835.1:c.*757-1723T= ENSP00000504343.1:n.*757-1723T=
ENST00000679088.1:c.*418T= ENSP00000504727.1:n.*418T=
ENST00000679098.1:c.*8+410T= ENSP00000504303.1:n.*8+410T=
ENST00000366782.5:c.*418T= ENSP00000355746.1:n.*418T=
ENST00000366783.7:c.*418T= ENSP00000355747.3:n.*418T=
ENST00000626989.2:c.1864T= ENSP00000486498.1:n.1864T=
NM_000447.2:c.*418T= NP_000438.2:n.*418T=
NM_012486.2:c.*418T= NP_036618.2:n.*418T=
XM_005273199.2:c.*418T= XP_005273256.1:n.*418T=
XM_011544236.1:c.*418T= XP_011542538.1:n.*418T=
XM_005273199.4:c.*418T= XP_005273256.1:n.*418T=
XM_017001835.1:c.*418T= XP_016857324.1:n.*418T=
XM_017001836.1:c.*418T= XP_016857325.1:n.*418T=
XR_001737316.2:n.1478-1723T=
XR_001737317.2:n.1478-1723T=
XR_001737318.2:n.2480T=
XR_001737319.1:n.2823T=
XR_001737320.1:n.2820T=
XR_001737321.1:n.2315T=
XR_949149.2:n.2477T=
XR_949150.3:n.2696T=
NM_000447.3:c.*418T= MANE Select NP_000438.2:n.*418T=
NM_012486.3:c.*418T= NP_036618.2:n.*418T=