Canonical Allele Identifier: CA345044807

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083156T>A (hg19) ; chr1:g.226895455T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895455T>A , CM000663.2:g.226895455T>A	GRCh38
NC_000001.10:g.227083156T>A , CM000663.1:g.227083156T>A	GRCh37
NC_000001.9:g.225149779T>A	NCBI36
NG_007381.1:g.29884T>A
NG_012825.2:g.2920T>A
NG_007381.2:g.30272T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1223T>A	ENSP00000355741.2:p.Val408Glu
ENST00000366782.6:c.1223T>A	ENSP00000355746.2:p.Val408Glu
ENST00000366783.8:c.1223T>A MANE Select	ENSP00000355747.3:p.Val408Glu
ENST00000471728.2:n.1861T>A
ENST00000524196.6:c.1223T>A	ENSP00000429036.2:p.Val408Glu
ENST00000626989.3:c.1223T>A	ENSP00000486498.2:p.Val408Glu
ENST00000676467.1:c.*1050T>A	ENSP00000504294.1:n.*1050T>A
ENST00000676747.1:c.1188+1330T>A	ENSP00000503244.1:n.1188+1330T>A
ENST00000676884.1:c.1223T>A	ENSP00000503200.1:p.Val408Glu
ENST00000676888.1:c.*564T>A	ENSP00000504483.1:n.*564T>A
ENST00000676907.1:c.*802T>A	ENSP00000504410.1:n.*802T>A
ENST00000676945.1:c.1191+1330T>A	ENSP00000504433.1:n.1191+1330T>A
ENST00000677065.1:n.1784T>A
ENST00000677414.1:c.1223T>A	ENSP00000503116.1:p.Val408Glu
ENST00000677529.1:n.2953T>A
ENST00000677596.1:c.*1445T>A	ENSP00000503618.1:n.*1445T>A
ENST00000677599.1:c.1191+1330T>A	ENSP00000503673.1:n.1191+1330T>A
ENST00000677748.1:n.3478T>A
ENST00000677880.1:c.788T>A	ENSP00000503121.1:p.Val263Glu
ENST00000678021.1:c.*846T>A	ENSP00000504674.1:n.*846T>A
ENST00000678233.1:c.1223T>A	ENSP00000504728.1:p.Val408Glu
ENST00000678320.1:c.1124T>A	ENSP00000503680.1:p.Val375Glu
ENST00000678655.1:c.1092+1330T>A	ENSP00000504230.1:n.1092+1330T>A
ENST00000678706.1:c.*600T>A	ENSP00000503659.1:n.*600T>A
ENST00000678776.1:c.*1360T>A	ENSP00000504624.1:n.*1360T>A
ENST00000678784.1:c.1073-2265T>A	ENSP00000504652.1:n.1073-2265T>A
ENST00000678820.1:c.1089+1330T>A	ENSP00000504138.1:n.1089+1330T>A
ENST00000678835.1:c.*757-2265T>A	ENSP00000504343.1:n.*757-2265T>A
ENST00000679088.1:c.1223T>A	ENSP00000504727.1:p.Val408Glu
ENST00000679098.1:c.1223T>A	ENSP00000504303.1:p.Val408Glu
ENST00000366782.5:c.1322T>A	ENSP00000355746.1:p.Val441Glu
ENST00000366783.7:c.1223T>A	ENSP00000355747.3:p.Val408Glu
ENST00000422240.6:c.1220T>A	ENSP00000403737.2:p.Val407Glu
ENST00000471728.1:n.481T>A
ENST00000472139.2:c.791T>A	ENSP00000427806.1:p.Val264Glu
ENST00000626989.2:c.1322T>A	ENSP00000486498.1:p.Val441Glu
NM_000447.2:c.1223T>A	NP_000438.2:p.Val408Glu
NM_012486.2:c.1220T>A	NP_036618.2:p.Val407Glu
XM_005273199.2:c.1223T>A	XP_005273256.1:p.Val408Glu
XM_011544236.1:c.791T>A	XP_011542538.1:p.Val264Glu
XR_949149.1:n.1957T>A
XM_005273199.4:c.1223T>A	XP_005273256.1:p.Val408Glu
XM_017001835.1:c.1223T>A	XP_016857324.1:p.Val408Glu
XM_017001836.1:c.1220T>A	XP_016857325.1:p.Val407Glu
XR_001737316.2:n.1478-2265T>A
XR_001737317.2:n.1478-2265T>A
XR_001737318.2:n.1938T>A
XR_001737319.1:n.2281T>A
XR_001737320.1:n.2278T>A
XR_001737321.1:n.1773T>A
XR_949149.2:n.1935T>A
XR_949150.3:n.2154T>A
NM_000447.3:c.1223T>A MANE Select	NP_000438.2:p.Val408Glu
NM_012486.3:c.1220T>A	NP_036618.2:p.Val407Glu