Canonical Allele Identifier: CA38627502

Gene: PSEN2

Linked Data

• dbSNP Id: rs200536369
• gnomAD v4: 1-226895993-G-A
• MyVariant Identifiers: chr1:g.227083694G>A (hg19) ; chr1:g.226895993G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895993G>A , CM000663.2:g.226895993G>A	GRCh38
NC_000001.10:g.227083694G>A , CM000663.1:g.227083694G>A	GRCh37
NC_000001.9:g.225150317G>A	NCBI36
NG_007381.1:g.30422G>A
NG_012825.2:g.3458G>A
NG_007381.2:g.30810G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*414G>A	ENSP00000355741.2:n.*414G>A
ENST00000366782.6:c.*414G>A	ENSP00000355746.2:n.*414G>A
ENST00000366783.8:c.*414G>A MANE Select	ENSP00000355747.3:n.*414G>A
ENST00000471728.2:n.2399G>A
ENST00000524196.6:c.*414G>A	ENSP00000429036.2:n.*414G>A
ENST00000626989.3:c.*414G>A	ENSP00000486498.2:n.*414G>A
ENST00000676467.1:c.*1588G>A	ENSP00000504294.1:n.*1588G>A
ENST00000676747.1:c.1189-1727G>A	ENSP00000503244.1:n.1189-1727G>A
ENST00000676884.1:c.*414G>A	ENSP00000503200.1:n.*414G>A
ENST00000676888.1:c.*1102G>A	ENSP00000504483.1:n.*1102G>A
ENST00000676907.1:c.*1340G>A	ENSP00000504410.1:n.*1340G>A
ENST00000676945.1:c.1191+1868G>A	ENSP00000504433.1:n.1191+1868G>A
ENST00000677065.1:n.2322G>A
ENST00000677414.1:c.*414G>A	ENSP00000503116.1:n.*414G>A
ENST00000677529.1:n.3491G>A
ENST00000677596.1:c.*1983G>A	ENSP00000503618.1:n.*1983G>A
ENST00000677599.1:c.1191+1868G>A	ENSP00000503673.1:n.1191+1868G>A
ENST00000677748.1:n.4016G>A
ENST00000677880.1:c.*414G>A	ENSP00000503121.1:n.*414G>A
ENST00000678021.1:c.*1384G>A	ENSP00000504674.1:n.*1384G>A
ENST00000678233.1:c.*8+406G>A	ENSP00000504728.1:n.*8+406G>A
ENST00000678320.1:c.*414G>A	ENSP00000503680.1:n.*414G>A
ENST00000678655.1:c.1093-1727G>A	ENSP00000504230.1:n.1093-1727G>A
ENST00000678706.1:c.*1138G>A	ENSP00000503659.1:n.*1138G>A
ENST00000678776.1:c.*1898G>A	ENSP00000504624.1:n.*1898G>A
ENST00000678784.1:c.1073-1727G>A	ENSP00000504652.1:n.1073-1727G>A
ENST00000678820.1:c.1090-1727G>A	ENSP00000504138.1:n.1090-1727G>A
ENST00000678835.1:c.*757-1727G>A	ENSP00000504343.1:n.*757-1727G>A
ENST00000679088.1:c.*414G>A	ENSP00000504727.1:n.*414G>A
ENST00000679098.1:c.*8+406G>A	ENSP00000504303.1:n.*8+406G>A
ENST00000366782.5:c.*414G>A	ENSP00000355746.1:n.*414G>A
ENST00000366783.7:c.*414G>A	ENSP00000355747.3:n.*414G>A
ENST00000626989.2:c.1860G>A	ENSP00000486498.1:n.1860G>A
NM_000447.2:c.*414G>A	NP_000438.2:n.*414G>A
NM_012486.2:c.*414G>A	NP_036618.2:n.*414G>A
XM_005273199.2:c.*414G>A	XP_005273256.1:n.*414G>A
XM_011544236.1:c.*414G>A	XP_011542538.1:n.*414G>A
XM_005273199.4:c.*414G>A	XP_005273256.1:n.*414G>A
XM_017001835.1:c.*414G>A	XP_016857324.1:n.*414G>A
XM_017001836.1:c.*414G>A	XP_016857325.1:n.*414G>A
XR_001737316.2:n.1478-1727G>A
XR_001737317.2:n.1478-1727G>A
XR_001737318.2:n.2476G>A
XR_001737319.1:n.2819G>A
XR_001737320.1:n.2816G>A
XR_001737321.1:n.2311G>A
XR_949149.2:n.2473G>A
XR_949150.3:n.2692G>A
NM_000447.3:c.*414G>A MANE Select	NP_000438.2:n.*414G>A
NM_012486.3:c.*414G>A	NP_036618.2:n.*414G>A