Canonical Allele Identifier: CA345045391

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083225A>T (hg19) ; chr1:g.226895524A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895524A>T , CM000663.2:g.226895524A>T	GRCh38
NC_000001.10:g.227083225A>T , CM000663.1:g.227083225A>T	GRCh37
NC_000001.9:g.225149848A>T	NCBI36
NG_007381.1:g.29953A>T
NG_012825.2:g.2989A>T
NG_007381.2:g.30341A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366779.6:c.1292A>T	ENSP00000355741.2:p.Asp431Val
ENST00000366782.6:c.1292A>T	ENSP00000355746.2:p.Asp431Val
ENST00000366783.8:c.1292A>T MANE Select	ENSP00000355747.3:p.Asp431Val
ENST00000471728.2:n.1930A>T
ENST00000524196.6:c.1292A>T	ENSP00000429036.2:p.Asp431Val
ENST00000626989.3:c.1292A>T	ENSP00000486498.2:p.Asp431Val
ENST00000676467.1:c.*1119A>T	ENSP00000504294.1:n.*1119A>T
ENST00000676747.1:c.1188+1399A>T	ENSP00000503244.1:n.1188+1399A>T
ENST00000676884.1:c.1292A>T	ENSP00000503200.1:p.Asp431Val
ENST00000676888.1:c.*633A>T	ENSP00000504483.1:n.*633A>T
ENST00000676907.1:c.*871A>T	ENSP00000504410.1:n.*871A>T
ENST00000676945.1:c.1191+1399A>T	ENSP00000504433.1:n.1191+1399A>T
ENST00000677065.1:n.1853A>T
ENST00000677414.1:c.1292A>T	ENSP00000503116.1:p.Asp431Val
ENST00000677529.1:n.3022A>T
ENST00000677596.1:c.*1514A>T	ENSP00000503618.1:n.*1514A>T
ENST00000677599.1:c.1191+1399A>T	ENSP00000503673.1:n.1191+1399A>T
ENST00000677748.1:n.3547A>T
ENST00000677880.1:c.857A>T	ENSP00000503121.1:p.Asp286Val
ENST00000678021.1:c.*915A>T	ENSP00000504674.1:n.*915A>T
ENST00000678233.1:c.1292A>T	ENSP00000504728.1:p.Asp431Val
ENST00000678320.1:c.1193A>T	ENSP00000503680.1:p.Asp398Val
ENST00000678655.1:c.1092+1399A>T	ENSP00000504230.1:n.1092+1399A>T
ENST00000678706.1:c.*669A>T	ENSP00000503659.1:n.*669A>T
ENST00000678776.1:c.*1429A>T	ENSP00000504624.1:n.*1429A>T
ENST00000678784.1:c.1073-2196A>T	ENSP00000504652.1:n.1073-2196A>T
ENST00000678820.1:c.1089+1399A>T	ENSP00000504138.1:n.1089+1399A>T
ENST00000678835.1:c.*757-2196A>T	ENSP00000504343.1:n.*757-2196A>T
ENST00000679088.1:c.1292A>T	ENSP00000504727.1:p.Asp431Val
ENST00000679098.1:c.1292A>T	ENSP00000504303.1:p.Asp431Val
ENST00000366782.5:c.1391A>T	ENSP00000355746.1:p.Asp464Val
ENST00000366783.7:c.1292A>T	ENSP00000355747.3:p.Asp431Val
ENST00000422240.6:c.1289A>T	ENSP00000403737.2:p.Asp430Val
ENST00000471728.1:n.550A>T
ENST00000472139.2:c.860A>T	ENSP00000427806.1:p.Asp287Val
ENST00000626989.2:c.1391A>T	ENSP00000486498.1:p.Asp464Val
NM_000447.2:c.1292A>T	NP_000438.2:p.Asp431Val
NM_012486.2:c.1289A>T	NP_036618.2:p.Asp430Val
XM_005273199.2:c.1292A>T	XP_005273256.1:p.Asp431Val
XM_011544236.1:c.860A>T	XP_011542538.1:p.Asp287Val
XR_949149.1:n.2026A>T
XM_005273199.4:c.1292A>T	XP_005273256.1:p.Asp431Val
XM_017001835.1:c.1292A>T	XP_016857324.1:p.Asp431Val
XM_017001836.1:c.1289A>T	XP_016857325.1:p.Asp430Val
XR_001737316.2:n.1478-2196A>T
XR_001737317.2:n.1478-2196A>T
XR_001737318.2:n.2007A>T
XR_001737319.1:n.2350A>T
XR_001737320.1:n.2347A>T
XR_001737321.1:n.1842A>T
XR_949149.2:n.2004A>T
XR_949150.3:n.2223A>T
NM_000447.3:c.1292A>T MANE Select	NP_000438.2:p.Asp431Val
NM_012486.3:c.1289A>T	NP_036618.2:p.Asp430Val