Canonical Allele Identifier: CA345043926

Gene: PSEN2

Linked Data

• dbSNP Id: rs1449580232
• gnomAD v2: 1-227081728-G-A
• gnomAD v4: 1-226894027-G-A
• MyVariant Identifiers: chr1:g.227081728G>A (hg19) ; chr1:g.226894027G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894027G>A , CM000663.2:g.226894027G>A	GRCh38
NC_000001.10:g.227081728G>A , CM000663.1:g.227081728G>A	GRCh37
NC_000001.9:g.225148351G>A	NCBI36
NG_007381.1:g.28456G>A
NG_012825.2:g.1492G>A
NG_007381.2:g.28844G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1093G>A	ENSP00000355741.2:p.Gly365Arg
ENST00000366782.6:c.1093G>A	ENSP00000355746.2:p.Gly365Arg
ENST00000366783.8:c.1093G>A MANE Select	ENSP00000355747.3:p.Gly365Arg
ENST00000471728.2:n.1731G>A
ENST00000524196.6:c.1093G>A	ENSP00000429036.2:p.Gly365Arg
ENST00000626989.3:c.1093G>A	ENSP00000486498.2:p.Gly365Arg
ENST00000676467.1:c.*920G>A	ENSP00000504294.1:n.*920G>A
ENST00000676747.1:c.1090G>A	ENSP00000503244.1:p.Gly364Arg
ENST00000676884.1:c.1093G>A	ENSP00000503200.1:p.Gly365Arg
ENST00000676888.1:c.*434G>A	ENSP00000504483.1:n.*434G>A
ENST00000676907.1:c.*672G>A	ENSP00000504410.1:n.*672G>A
ENST00000676945.1:c.1093G>A	ENSP00000504433.1:p.Gly365Arg
ENST00000677065.1:n.1654G>A
ENST00000677414.1:c.1093G>A	ENSP00000503116.1:p.Gly365Arg
ENST00000677529.1:n.2823G>A
ENST00000677596.1:c.*1315G>A	ENSP00000503618.1:n.*1315G>A
ENST00000677599.1:c.1093G>A	ENSP00000503673.1:p.Gly365Arg
ENST00000677748.1:n.3348G>A
ENST00000677880.1:c.658G>A	ENSP00000503121.1:p.Gly220Arg
ENST00000678021.1:c.*716G>A	ENSP00000504674.1:n.*716G>A
ENST00000678233.1:c.1093G>A	ENSP00000504728.1:p.Gly365Arg
ENST00000678320.1:c.994G>A	ENSP00000503680.1:p.Gly332Arg
ENST00000678655.1:c.994G>A	ENSP00000504230.1:p.Gly332Arg
ENST00000678706.1:c.*470G>A	ENSP00000503659.1:n.*470G>A
ENST00000678776.1:c.*1230G>A	ENSP00000504624.1:n.*1230G>A
ENST00000678784.1:c.1072+2183G>A	ENSP00000504652.1:n.1072+2183G>A
ENST00000678820.1:c.991G>A	ENSP00000504138.1:p.Gly331Arg
ENST00000678835.1:c.*756+2183G>A	ENSP00000504343.1:n.*756+2183G>A
ENST00000679088.1:c.1093G>A	ENSP00000504727.1:p.Gly365Arg
ENST00000679098.1:c.1093G>A	ENSP00000504303.1:p.Gly365Arg
ENST00000366782.5:c.1192G>A	ENSP00000355746.1:p.Gly398Arg
ENST00000366783.7:c.1093G>A	ENSP00000355747.3:p.Gly365Arg
ENST00000422240.6:c.1090G>A	ENSP00000403737.2:p.Gly364Arg
ENST00000471728.1:n.351G>A
ENST00000472139.2:c.661G>A	ENSP00000427806.1:p.Gly221Arg
ENST00000626989.2:c.1192G>A	ENSP00000486498.1:p.Gly398Arg
NM_000447.2:c.1093G>A	NP_000438.2:p.Gly365Arg
NM_012486.2:c.1090G>A	NP_036618.2:p.Gly364Arg
XM_005273199.2:c.1093G>A	XP_005273256.1:p.Gly365Arg
XM_011544236.1:c.661G>A	XP_011542538.1:p.Gly221Arg
XR_949149.1:n.1827G>A
XM_005273199.4:c.1093G>A	XP_005273256.1:p.Gly365Arg
XM_017001835.1:c.1093G>A	XP_016857324.1:p.Gly365Arg
XM_017001836.1:c.1090G>A	XP_016857325.1:p.Gly364Arg
XR_001737316.2:n.1477+2183G>A
XR_001737317.2:n.1477+2183G>A
XR_001737318.2:n.1808G>A
XR_001737319.1:n.2151G>A
XR_001737320.1:n.2148G>A
XR_001737321.1:n.1643G>A
XR_949149.2:n.1805G>A
XR_949150.3:n.2024G>A
NM_000447.3:c.1093G>A MANE Select	NP_000438.2:p.Gly365Arg
NM_012486.3:c.1090G>A	NP_036618.2:p.Gly364Arg