Canonical Allele Identifier: CA2747997008

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226896008T>G , CM000663.2:g.226896008T>G	GRCh38
NC_000001.10:g.227083709T>G , CM000663.1:g.227083709T>G	GRCh37
NC_000001.9:g.225150332T>G	NCBI36
NG_007381.1:g.30437T>G
NG_012825.2:g.3473T>G
NG_007381.2:g.30825T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*429T>G	ENSP00000355741.2:n.*429T>G
ENST00000366782.6:c.*429T>G	ENSP00000355746.2:n.*429T>G
ENST00000366783.8:c.*429T>G MANE Select	ENSP00000355747.3:n.*429T>G
ENST00000471728.2:n.2414T>G
ENST00000524196.6:c.*429T>G	ENSP00000429036.2:n.*429T>G
ENST00000626989.3:c.*429T>G	ENSP00000486498.2:n.*429T>G
ENST00000676467.1:c.*1603T>G	ENSP00000504294.1:n.*1603T>G
ENST00000676747.1:c.1189-1712T>G	ENSP00000503244.1:n.1189-1712T>G
ENST00000676884.1:c.*429T>G	ENSP00000503200.1:n.*429T>G
ENST00000676888.1:c.*1117T>G	ENSP00000504483.1:n.*1117T>G
ENST00000676907.1:c.*1355T>G	ENSP00000504410.1:n.*1355T>G
ENST00000676945.1:c.1191+1883T>G	ENSP00000504433.1:n.1191+1883T>G
ENST00000677065.1:n.2337T>G
ENST00000677414.1:c.*429T>G	ENSP00000503116.1:n.*429T>G
ENST00000677529.1:n.3506T>G
ENST00000677596.1:c.*1998T>G	ENSP00000503618.1:n.*1998T>G
ENST00000677599.1:c.1191+1883T>G	ENSP00000503673.1:n.1191+1883T>G
ENST00000677748.1:n.4031T>G
ENST00000677880.1:c.*429T>G	ENSP00000503121.1:n.*429T>G
ENST00000678021.1:c.*1399T>G	ENSP00000504674.1:n.*1399T>G
ENST00000678233.1:c.*8+421T>G	ENSP00000504728.1:n.*8+421T>G
ENST00000678320.1:c.*429T>G	ENSP00000503680.1:n.*429T>G
ENST00000678655.1:c.1093-1712T>G	ENSP00000504230.1:n.1093-1712T>G
ENST00000678706.1:c.*1153T>G	ENSP00000503659.1:n.*1153T>G
ENST00000678776.1:c.*1913T>G	ENSP00000504624.1:n.*1913T>G
ENST00000678784.1:c.1073-1712T>G	ENSP00000504652.1:n.1073-1712T>G
ENST00000678820.1:c.1090-1712T>G	ENSP00000504138.1:n.1090-1712T>G
ENST00000678835.1:c.*757-1712T>G	ENSP00000504343.1:n.*757-1712T>G
ENST00000679088.1:c.*429T>G	ENSP00000504727.1:n.*429T>G
ENST00000679098.1:c.*8+421T>G	ENSP00000504303.1:n.*8+421T>G
ENST00000366782.5:c.*429T>G	ENSP00000355746.1:n.*429T>G
ENST00000366783.7:c.*429T>G	ENSP00000355747.3:n.*429T>G
ENST00000626989.2:c.1875T>G	ENSP00000486498.1:n.1875T>G
NM_000447.2:c.*429T>G	NP_000438.2:n.*429T>G
NM_012486.2:c.*429T>G	NP_036618.2:n.*429T>G
XM_005273199.2:c.*429T>G	XP_005273256.1:n.*429T>G
XM_011544236.1:c.*429T>G	XP_011542538.1:n.*429T>G
XM_005273199.4:c.*429T>G	XP_005273256.1:n.*429T>G
XM_017001835.1:c.*429T>G	XP_016857324.1:n.*429T>G
XM_017001836.1:c.*429T>G	XP_016857325.1:n.*429T>G
XR_001737316.2:n.1478-1712T>G
XR_001737317.2:n.1478-1712T>G
XR_001737318.2:n.2491T>G
XR_001737319.1:n.2834T>G
XR_001737320.1:n.2831T>G
XR_001737321.1:n.2326T>G
XR_949149.2:n.2488T>G
XR_949150.3:n.2707T>G
NM_000447.3:c.*429T>G MANE Select	NP_000438.2:n.*429T>G
NM_012486.3:c.*429T>G	NP_036618.2:n.*429T>G