Canonical Allele Identifier: CA345044999

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226895476-C-G
• MyVariant Identifiers: chr1:g.227083177C>G (hg19) ; chr1:g.226895476C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895476C>G , CM000663.2:g.226895476C>G	GRCh38
NC_000001.10:g.227083177C>G , CM000663.1:g.227083177C>G	GRCh37
NC_000001.9:g.225149800C>G	NCBI36
NG_007381.1:g.29905C>G
NG_012825.2:g.2941C>G
NG_007381.2:g.30293C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1244C>G	ENSP00000355741.2:p.Ala415Gly
ENST00000366782.6:c.1244C>G	ENSP00000355746.2:p.Ala415Gly
ENST00000366783.8:c.1244C>G MANE Select	ENSP00000355747.3:p.Ala415Gly
ENST00000471728.2:n.1882C>G
ENST00000524196.6:c.1244C>G	ENSP00000429036.2:p.Ala415Gly
ENST00000626989.3:c.1244C>G	ENSP00000486498.2:p.Ala415Gly
ENST00000676467.1:c.*1071C>G	ENSP00000504294.1:n.*1071C>G
ENST00000676747.1:c.1188+1351C>G	ENSP00000503244.1:n.1188+1351C>G
ENST00000676884.1:c.1244C>G	ENSP00000503200.1:p.Ala415Gly
ENST00000676888.1:c.*585C>G	ENSP00000504483.1:n.*585C>G
ENST00000676907.1:c.*823C>G	ENSP00000504410.1:n.*823C>G
ENST00000676945.1:c.1191+1351C>G	ENSP00000504433.1:n.1191+1351C>G
ENST00000677065.1:n.1805C>G
ENST00000677414.1:c.1244C>G	ENSP00000503116.1:p.Ala415Gly
ENST00000677529.1:n.2974C>G
ENST00000677596.1:c.*1466C>G	ENSP00000503618.1:n.*1466C>G
ENST00000677599.1:c.1191+1351C>G	ENSP00000503673.1:n.1191+1351C>G
ENST00000677748.1:n.3499C>G
ENST00000677880.1:c.809C>G	ENSP00000503121.1:p.Ala270Gly
ENST00000678021.1:c.*867C>G	ENSP00000504674.1:n.*867C>G
ENST00000678233.1:c.1244C>G	ENSP00000504728.1:p.Ala415Gly
ENST00000678320.1:c.1145C>G	ENSP00000503680.1:p.Ala382Gly
ENST00000678655.1:c.1092+1351C>G	ENSP00000504230.1:n.1092+1351C>G
ENST00000678706.1:c.*621C>G	ENSP00000503659.1:n.*621C>G
ENST00000678776.1:c.*1381C>G	ENSP00000504624.1:n.*1381C>G
ENST00000678784.1:c.1073-2244C>G	ENSP00000504652.1:n.1073-2244C>G
ENST00000678820.1:c.1089+1351C>G	ENSP00000504138.1:n.1089+1351C>G
ENST00000678835.1:c.*757-2244C>G	ENSP00000504343.1:n.*757-2244C>G
ENST00000679088.1:c.1244C>G	ENSP00000504727.1:p.Ala415Gly
ENST00000679098.1:c.1244C>G	ENSP00000504303.1:p.Ala415Gly
ENST00000366782.5:c.1343C>G	ENSP00000355746.1:p.Ala448Gly
ENST00000366783.7:c.1244C>G	ENSP00000355747.3:p.Ala415Gly
ENST00000422240.6:c.1241C>G	ENSP00000403737.2:p.Ala414Gly
ENST00000471728.1:n.502C>G
ENST00000472139.2:c.812C>G	ENSP00000427806.1:p.Ala271Gly
ENST00000626989.2:c.1343C>G	ENSP00000486498.1:p.Ala448Gly
NM_000447.2:c.1244C>G	NP_000438.2:p.Ala415Gly
NM_012486.2:c.1241C>G	NP_036618.2:p.Ala414Gly
XM_005273199.2:c.1244C>G	XP_005273256.1:p.Ala415Gly
XM_011544236.1:c.812C>G	XP_011542538.1:p.Ala271Gly
XR_949149.1:n.1978C>G
XM_005273199.4:c.1244C>G	XP_005273256.1:p.Ala415Gly
XM_017001835.1:c.1244C>G	XP_016857324.1:p.Ala415Gly
XM_017001836.1:c.1241C>G	XP_016857325.1:p.Ala414Gly
XR_001737316.2:n.1478-2244C>G
XR_001737317.2:n.1478-2244C>G
XR_001737318.2:n.1959C>G
XR_001737319.1:n.2302C>G
XR_001737320.1:n.2299C>G
XR_001737321.1:n.1794C>G
XR_949149.2:n.1956C>G
XR_949150.3:n.2175C>G
NM_000447.3:c.1244C>G MANE Select	NP_000438.2:p.Ala415Gly
NM_012486.3:c.1241C>G	NP_036618.2:p.Ala414Gly