Canonical Allele Identifier: CA1424571
Gene: PSEN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2727425
ClinVar RCV Id: RCV003511249
dbSNP Id: rs371686514

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226888158G>C , CM000663.2:g.226888158G>C GRCh38
NC_000001.10:g.227075859G>C , CM000663.1:g.227075859G>C GRCh37
NC_000001.9:g.225142482G>C NCBI36
NG_007381.1:g.22587G>C
NG_007381.2:g.22975G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.566G>C ENSP00000355741.2:p.Gly189Ala
ENST00000366782.6:c.566G>C ENSP00000355746.2:p.Gly189Ala
ENST00000366783.8:c.566G>C MANE Select ENSP00000355747.3:p.Gly189Ala
ENST00000524196.6:c.566G>C ENSP00000429036.2:p.Gly189Ala
ENST00000626989.3:c.566G>C ENSP00000486498.2:p.Gly189Ala
ENST00000676467.1:c.*396G>C ENSP00000504294.1:n.*396G>C
ENST00000676747.1:c.566G>C ENSP00000503244.1:p.Gly189Ala
ENST00000676840.1:c.566G>C ENSP00000504318.1:p.Gly189Ala
ENST00000676884.1:c.566G>C ENSP00000503200.1:p.Gly189Ala
ENST00000676888.1:c.566G>C ENSP00000504483.1:p.Gly189Ala
ENST00000676907.1:c.*145G>C ENSP00000504410.1:n.*145G>C
ENST00000676945.1:c.566G>C ENSP00000504433.1:p.Gly189Ala
ENST00000677065.1:n.1127G>C
ENST00000677414.1:c.566G>C ENSP00000503116.1:p.Gly189Ala
ENST00000677529.1:n.1004G>C
ENST00000677596.1:c.*473G>C ENSP00000503618.1:n.*473G>C
ENST00000677599.1:c.566G>C ENSP00000503673.1:p.Gly189Ala
ENST00000677748.1:n.1004G>C
ENST00000677880.1:c.134G>C ENSP00000503121.1:p.Gly45Ala
ENST00000678021.1:c.*189G>C ENSP00000504674.1:n.*189G>C
ENST00000678233.1:c.566G>C ENSP00000504728.1:p.Gly189Ala
ENST00000678320.1:c.566G>C ENSP00000503680.1:p.Gly189Ala
ENST00000678655.1:c.566G>C ENSP00000504230.1:p.Gly189Ala
ENST00000678706.1:c.566G>C ENSP00000503659.1:p.Gly189Ala
ENST00000678776.1:c.*396G>C ENSP00000504624.1:n.*396G>C
ENST00000678784.1:c.566G>C ENSP00000504652.1:p.Gly189Ala
ENST00000678820.1:c.566G>C ENSP00000504138.1:p.Gly189Ala
ENST00000678835.1:c.566G>C ENSP00000504343.1:p.Gly189Ala
ENST00000679088.1:c.566G>C ENSP00000504727.1:p.Gly189Ala
ENST00000679098.1:c.566G>C ENSP00000504303.1:p.Gly189Ala
ENST00000366782.5:c.665G>C ENSP00000355746.1:p.Gly222Ala
ENST00000366783.7:c.566G>C ENSP00000355747.3:p.Gly189Ala
ENST00000422240.6:c.566G>C ENSP00000403737.2:p.Gly189Ala
ENST00000460775.5:c.47G>C ENSP00000427912.1:p.Gly16Ala
ENST00000472139.2:c.134G>C ENSP00000427806.1:p.Gly45Ala
ENST00000626989.2:c.665G>C ENSP00000486498.1:p.Gly222Ala
NM_000447.2:c.566G>C NP_000438.2:p.Gly189Ala
NM_012486.2:c.566G>C NP_036618.2:p.Gly189Ala
XM_005273199.2:c.566G>C XP_005273256.1:p.Gly189Ala
XM_011544236.1:c.134G>C XP_011542538.1:p.Gly45Ala
XR_949149.1:n.993G>C
XR_949150.1:n.993G>C
XM_005273199.4:c.566G>C XP_005273256.1:p.Gly189Ala
XM_017001835.1:c.566G>C XP_016857324.1:p.Gly189Ala
XM_017001836.1:c.566G>C XP_016857325.1:p.Gly189Ala
XR_001737316.2:n.971G>C
XR_001737317.2:n.971G>C
XR_001737318.2:n.971G>C
XR_001737319.1:n.1314G>C
XR_001737320.1:n.1314G>C
XR_001737321.1:n.806G>C
XR_949149.2:n.971G>C
XR_949150.3:n.971G>C
NM_000447.3:c.566G>C MANE Select NP_000438.2:p.Gly189Ala
NM_012486.3:c.566G>C NP_036618.2:p.Gly189Ala