Canonical Allele Identifier: CA1225082464
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226888852T= , CM000663.2:g.226888852T= GRCh38
NC_000001.10:g.227076553T= , CM000663.1:g.227076553T= GRCh37
NC_000001.9:g.225143176T= NCBI36
NG_007381.1:g.23281T=
NG_007381.2:g.23669T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.590T= ENSP00000355741.2:p.Val197=
ENST00000366782.6:c.590T= ENSP00000355746.2:p.Val197=
ENST00000366783.8:c.590T= MANE Select ENSP00000355747.3:p.Val197=
ENST00000524196.6:c.590T= ENSP00000429036.2:p.Val197=
ENST00000626989.3:c.590T= ENSP00000486498.2:p.Val197=
ENST00000676467.1:c.*420T= ENSP00000504294.1:n.*420T=
ENST00000676747.1:c.590T= ENSP00000503244.1:p.Val197=
ENST00000676840.1:c.590T= ENSP00000504318.1:p.Val197=
ENST00000676884.1:c.590T= ENSP00000503200.1:p.Val197=
ENST00000676888.1:c.590T= ENSP00000504483.1:p.Val197=
ENST00000676907.1:c.*169T= ENSP00000504410.1:n.*169T=
ENST00000676945.1:c.590T= ENSP00000504433.1:p.Val197=
ENST00000677065.1:n.1151T=
ENST00000677414.1:c.590T= ENSP00000503116.1:p.Val197=
ENST00000677529.1:n.1028T=
ENST00000677596.1:c.*497T= ENSP00000503618.1:n.*497T=
ENST00000677599.1:c.590T= ENSP00000503673.1:p.Val197=
ENST00000677748.1:n.1028T=
ENST00000677880.1:c.158T= ENSP00000503121.1:p.Val53=
ENST00000678021.1:c.*213T= ENSP00000504674.1:n.*213T=
ENST00000678233.1:c.590T= ENSP00000504728.1:p.Val197=
ENST00000678320.1:c.590T= ENSP00000503680.1:p.Val197=
ENST00000678655.1:c.590T= ENSP00000504230.1:p.Val197=
ENST00000678706.1:c.590T= ENSP00000503659.1:p.Val197=
ENST00000678776.1:c.*420T= ENSP00000504624.1:n.*420T=
ENST00000678784.1:c.590T= ENSP00000504652.1:p.Val197=
ENST00000678820.1:c.590T= ENSP00000504138.1:p.Val197=
ENST00000678835.1:c.590T= ENSP00000504343.1:p.Val197=
ENST00000679088.1:c.590T= ENSP00000504727.1:p.Val197=
ENST00000679098.1:c.590T= ENSP00000504303.1:p.Val197=
ENST00000366782.5:c.689T= ENSP00000355746.1:p.Val230=
ENST00000366783.7:c.590T= ENSP00000355747.3:p.Val197=
ENST00000422240.6:c.590T= ENSP00000403737.2:p.Val197=
ENST00000460775.5:c.71T= ENSP00000427912.1:p.Val24=
ENST00000472139.2:c.158T= ENSP00000427806.1:p.Val53=
ENST00000626989.2:c.689T= ENSP00000486498.1:p.Val230=
NM_000447.2:c.590T= NP_000438.2:p.Val197=
NM_012486.2:c.590T= NP_036618.2:p.Val197=
XM_005273199.2:c.590T= XP_005273256.1:p.Val197=
XM_011544236.1:c.158T= XP_011542538.1:p.Val53=
XR_949149.1:n.1017T=
XR_949150.1:n.1017T=
XM_005273199.4:c.590T= XP_005273256.1:p.Val197=
XM_017001835.1:c.590T= XP_016857324.1:p.Val197=
XM_017001836.1:c.590T= XP_016857325.1:p.Val197=
XR_001737316.2:n.995T=
XR_001737317.2:n.995T=
XR_001737318.2:n.995T=
XR_001737319.1:n.1338T=
XR_001737320.1:n.1338T=
XR_001737321.1:n.830T=
XR_949149.2:n.995T=
XR_949150.3:n.995T=
NM_000447.3:c.590T= MANE Select NP_000438.2:p.Val197=
NM_012486.3:c.590T= NP_036618.2:p.Val197=