Canonical Allele Identifier: CA345045551

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083243T>G (hg19) ; chr1:g.226895542T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895542T>G , CM000663.2:g.226895542T>G	GRCh38
NC_000001.10:g.227083243T>G , CM000663.1:g.227083243T>G	GRCh37
NC_000001.9:g.225149866T>G	NCBI36
NG_007381.1:g.29971T>G
NG_012825.2:g.3007T>G
NG_007381.2:g.30359T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1310T>G	ENSP00000355741.2:p.Phe437Cys
ENST00000366782.6:c.1310T>G	ENSP00000355746.2:p.Phe437Cys
ENST00000366783.8:c.1310T>G MANE Select	ENSP00000355747.3:p.Phe437Cys
ENST00000471728.2:n.1948T>G
ENST00000524196.6:c.1310T>G	ENSP00000429036.2:p.Phe437Cys
ENST00000626989.3:c.1310T>G	ENSP00000486498.2:p.Phe437Cys
ENST00000676467.1:c.*1137T>G	ENSP00000504294.1:n.*1137T>G
ENST00000676747.1:c.1188+1417T>G	ENSP00000503244.1:n.1188+1417T>G
ENST00000676884.1:c.1310T>G	ENSP00000503200.1:p.Phe437Cys
ENST00000676888.1:c.*651T>G	ENSP00000504483.1:n.*651T>G
ENST00000676907.1:c.*889T>G	ENSP00000504410.1:n.*889T>G
ENST00000676945.1:c.1191+1417T>G	ENSP00000504433.1:n.1191+1417T>G
ENST00000677065.1:n.1871T>G
ENST00000677414.1:c.1310T>G	ENSP00000503116.1:p.Phe437Cys
ENST00000677529.1:n.3040T>G
ENST00000677596.1:c.*1532T>G	ENSP00000503618.1:n.*1532T>G
ENST00000677599.1:c.1191+1417T>G	ENSP00000503673.1:n.1191+1417T>G
ENST00000677748.1:n.3565T>G
ENST00000677880.1:c.875T>G	ENSP00000503121.1:p.Phe292Cys
ENST00000678021.1:c.*933T>G	ENSP00000504674.1:n.*933T>G
ENST00000678233.1:c.1310T>G	ENSP00000504728.1:p.Phe437Cys
ENST00000678320.1:c.1211T>G	ENSP00000503680.1:p.Phe404Cys
ENST00000678655.1:c.1092+1417T>G	ENSP00000504230.1:n.1092+1417T>G
ENST00000678706.1:c.*687T>G	ENSP00000503659.1:n.*687T>G
ENST00000678776.1:c.*1447T>G	ENSP00000504624.1:n.*1447T>G
ENST00000678784.1:c.1073-2178T>G	ENSP00000504652.1:n.1073-2178T>G
ENST00000678820.1:c.1089+1417T>G	ENSP00000504138.1:n.1089+1417T>G
ENST00000678835.1:c.*757-2178T>G	ENSP00000504343.1:n.*757-2178T>G
ENST00000679088.1:c.1310T>G	ENSP00000504727.1:p.Phe437Cys
ENST00000679098.1:c.1310T>G	ENSP00000504303.1:p.Phe437Cys
ENST00000366782.5:c.1409T>G	ENSP00000355746.1:p.Phe470Cys
ENST00000366783.7:c.1310T>G	ENSP00000355747.3:p.Phe437Cys
ENST00000422240.6:c.1307T>G	ENSP00000403737.2:p.Phe436Cys
ENST00000471728.1:n.568T>G
ENST00000472139.2:c.878T>G	ENSP00000427806.1:p.Phe293Cys
ENST00000626989.2:c.1409T>G	ENSP00000486498.1:p.Phe470Cys
NM_000447.2:c.1310T>G	NP_000438.2:p.Phe437Cys
NM_012486.2:c.1307T>G	NP_036618.2:p.Phe436Cys
XM_005273199.2:c.1310T>G	XP_005273256.1:p.Phe437Cys
XM_011544236.1:c.878T>G	XP_011542538.1:p.Phe293Cys
XR_949149.1:n.2044T>G
XM_005273199.4:c.1310T>G	XP_005273256.1:p.Phe437Cys
XM_017001835.1:c.1310T>G	XP_016857324.1:p.Phe437Cys
XM_017001836.1:c.1307T>G	XP_016857325.1:p.Phe436Cys
XR_001737316.2:n.1478-2178T>G
XR_001737317.2:n.1478-2178T>G
XR_001737318.2:n.2025T>G
XR_001737319.1:n.2368T>G
XR_001737320.1:n.2365T>G
XR_001737321.1:n.1860T>G
XR_949149.2:n.2022T>G
XR_949150.3:n.2241T>G
NM_000447.3:c.1310T>G MANE Select	NP_000438.2:p.Phe437Cys
NM_012486.3:c.1307T>G	NP_036618.2:p.Phe436Cys