Canonical Allele Identifier: CA1225085486
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895958A= , CM000663.2:g.226895958A= GRCh38
NC_000001.10:g.227083659A= , CM000663.1:g.227083659A= GRCh37
NC_000001.9:g.225150282A= NCBI36
NG_007381.1:g.30387A=
NG_012825.2:g.3423A=
NG_007381.2:g.30775A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.*379A= ENSP00000355741.2:n.*379A=
ENST00000366782.6:c.*379A= ENSP00000355746.2:n.*379A=
ENST00000366783.8:c.*379A= MANE Select ENSP00000355747.3:n.*379A=
ENST00000471728.2:n.2364A=
ENST00000524196.6:c.*379A= ENSP00000429036.2:n.*379A=
ENST00000626989.3:c.*379A= ENSP00000486498.2:n.*379A=
ENST00000676467.1:c.*1553A= ENSP00000504294.1:n.*1553A=
ENST00000676747.1:c.1189-1762A= ENSP00000503244.1:n.1189-1762A=
ENST00000676884.1:c.*379A= ENSP00000503200.1:n.*379A=
ENST00000676888.1:c.*1067A= ENSP00000504483.1:n.*1067A=
ENST00000676907.1:c.*1305A= ENSP00000504410.1:n.*1305A=
ENST00000676945.1:c.1191+1833A= ENSP00000504433.1:n.1191+1833A=
ENST00000677065.1:n.2287A=
ENST00000677414.1:c.*379A= ENSP00000503116.1:n.*379A=
ENST00000677529.1:n.3456A=
ENST00000677596.1:c.*1948A= ENSP00000503618.1:n.*1948A=
ENST00000677599.1:c.1191+1833A= ENSP00000503673.1:n.1191+1833A=
ENST00000677748.1:n.3981A=
ENST00000677880.1:c.*379A= ENSP00000503121.1:n.*379A=
ENST00000678021.1:c.*1349A= ENSP00000504674.1:n.*1349A=
ENST00000678233.1:c.*8+371A= ENSP00000504728.1:n.*8+371A=
ENST00000678320.1:c.*379A= ENSP00000503680.1:n.*379A=
ENST00000678655.1:c.1093-1762A= ENSP00000504230.1:n.1093-1762A=
ENST00000678706.1:c.*1103A= ENSP00000503659.1:n.*1103A=
ENST00000678776.1:c.*1863A= ENSP00000504624.1:n.*1863A=
ENST00000678784.1:c.1073-1762A= ENSP00000504652.1:n.1073-1762A=
ENST00000678820.1:c.1090-1762A= ENSP00000504138.1:n.1090-1762A=
ENST00000678835.1:c.*757-1762A= ENSP00000504343.1:n.*757-1762A=
ENST00000679088.1:c.*379A= ENSP00000504727.1:n.*379A=
ENST00000679098.1:c.*8+371A= ENSP00000504303.1:n.*8+371A=
ENST00000366782.5:c.*379A= ENSP00000355746.1:n.*379A=
ENST00000366783.7:c.*379A= ENSP00000355747.3:n.*379A=
ENST00000626989.2:c.1825A= ENSP00000486498.1:n.1825A=
NM_000447.2:c.*379A= NP_000438.2:n.*379A=
NM_012486.2:c.*379A= NP_036618.2:n.*379A=
XM_005273199.2:c.*379A= XP_005273256.1:n.*379A=
XM_011544236.1:c.*379A= XP_011542538.1:n.*379A=
XM_005273199.4:c.*379A= XP_005273256.1:n.*379A=
XM_017001835.1:c.*379A= XP_016857324.1:n.*379A=
XM_017001836.1:c.*379A= XP_016857325.1:n.*379A=
XR_001737316.2:n.1478-1762A=
XR_001737317.2:n.1478-1762A=
XR_001737318.2:n.2441A=
XR_001737319.1:n.2784A=
XR_001737320.1:n.2781A=
XR_001737321.1:n.2276A=
XR_949149.2:n.2438A=
XR_949150.3:n.2657A=
NM_000447.3:c.*379A= MANE Select NP_000438.2:n.*379A=
NM_012486.3:c.*379A= NP_036618.2:n.*379A=