Canonical Allele Identifier: CA2650788605
Gene: PSEN2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226896058_226896059insTGCCATATATTTTTAAGACTTTTCTTTC , CM000663.2:g.226896058_226896059insTGCCATATATTTTTAAGACTTTTCTTTC GRCh38
NC_000001.10:g.227083759_227083760insTGCCATATATTTTTAAGACTTTTCTTTC , CM000663.1:g.227083759_227083760insTGCCATATATTTTTAAGACTTTTCTTTC GRCh37
NC_000001.9:g.225150382_225150383insTGCCATATATTTTTAAGACTTTTCTTTC NCBI36
NG_007381.1:g.30487_30488insTGCCATATATTTTTAAGACTTTTCTTTC
NG_012825.2:g.3523_3524insTGCCATATATTTTTAAGACTTTTCTTTC
NG_007381.2:g.30875_30876insTGCCATATATTTTTAAGACTTTTCTTTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000355741.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000366782.6:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000355746.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000366783.8:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC MANE Select ENSP00000355747.3:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000471728.2:n.2464_2465insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000524196.6:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000429036.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000626989.3:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000486498.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000676467.1:c.*1653_*1654insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504294.1:n.*1653_*1654insTGCCATATATTTTTAAGACTTTTCTTT...
ENST00000676747.1:c.1189-1662_1189-1661insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503244.1:n.1189-1662_1189-1661insTGCCATATATTTTTAAGAC...
ENST00000676884.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503200.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000676888.1:c.*1167_*1168insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504483.1:n.*1167_*1168insTGCCATATATTTTTAAGACTTTTCTTT...
ENST00000676907.1:c.*1405_*1406insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504410.1:n.*1405_*1406insTGCCATATATTTTTAAGACTTTTCTTT...
ENST00000676945.1:c.1191+1933_1191+1934insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504433.1:n.1191+1933_1191+1934insTGCCATATATTTTTAAGAC...
ENST00000677065.1:n.2387_2388insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000677414.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503116.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000677529.1:n.3556_3557insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000677596.1:c.*2048_*2049insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503618.1:n.*2048_*2049insTGCCATATATTTTTAAGACTTTTCTTT...
ENST00000677599.1:c.1191+1933_1191+1934insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503673.1:n.1191+1933_1191+1934insTGCCATATATTTTTAAGAC...
ENST00000677748.1:n.4081_4082insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000677880.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503121.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000678021.1:c.*1449_*1450insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504674.1:n.*1449_*1450insTGCCATATATTTTTAAGACTTTTCTTT...
ENST00000678233.1:c.*8+471_*8+472insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504728.1:n.*8+471_*8+472insTGCCATATATTTTTAAGACTTTTCT...
ENST00000678320.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503680.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000678655.1:c.1093-1662_1093-1661insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504230.1:n.1093-1662_1093-1661insTGCCATATATTTTTAAGAC...
ENST00000678706.1:c.*1203_*1204insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000503659.1:n.*1203_*1204insTGCCATATATTTTTAAGACTTTTCTTT...
ENST00000678776.1:c.*1963_*1964insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504624.1:n.*1963_*1964insTGCCATATATTTTTAAGACTTTTCTTT...
ENST00000678784.1:c.1073-1662_1073-1661insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504652.1:n.1073-1662_1073-1661insTGCCATATATTTTTAAGAC...
ENST00000678820.1:c.1090-1662_1090-1661insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504138.1:n.1090-1662_1090-1661insTGCCATATATTTTTAAGAC...
ENST00000678835.1:c.*757-1662_*757-1661insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504343.1:n.*757-1662_*757-1661insTGCCATATATTTTTAAGAC...
ENST00000679088.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504727.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000679098.1:c.*8+471_*8+472insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000504303.1:n.*8+471_*8+472insTGCCATATATTTTTAAGACTTTTCT...
ENST00000366782.5:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000355746.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000366783.7:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000355747.3:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
ENST00000626989.2:c.1925_1926insTGCCATATATTTTTAAGACTTTTCTTTC ENSP00000486498.1:n.1925_1926insTGCCATATATTTTTAAGACTTTTCTTTC
NM_000447.2:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC NP_000438.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
NM_012486.2:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC NP_036618.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
XM_005273199.2:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC XP_005273256.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
XM_011544236.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC XP_011542538.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
XM_005273199.4:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC XP_005273256.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
XM_017001835.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC XP_016857324.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
XM_017001836.1:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC XP_016857325.1:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
XR_001737316.2:n.1478-1662_1478-1661insTGCCATATATTTTTAAGACTTTTCTTTC
XR_001737317.2:n.1478-1662_1478-1661insTGCCATATATTTTTAAGACTTTTCTTTC
XR_001737318.2:n.2541_2542insTGCCATATATTTTTAAGACTTTTCTTTC
XR_001737319.1:n.2884_2885insTGCCATATATTTTTAAGACTTTTCTTTC
XR_001737320.1:n.2881_2882insTGCCATATATTTTTAAGACTTTTCTTTC
XR_001737321.1:n.2376_2377insTGCCATATATTTTTAAGACTTTTCTTTC
XR_949149.2:n.2538_2539insTGCCATATATTTTTAAGACTTTTCTTTC
XR_949150.3:n.2757_2758insTGCCATATATTTTTAAGACTTTTCTTTC
NM_000447.3:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC MANE Select NP_000438.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC
NM_012486.3:c.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC NP_036618.2:n.*479_*480insTGCCATATATTTTTAAGACTTTTCTTTC