Canonical Allele Identifier: CA423520454

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083139C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895438C>A , CM000663.2:g.226895438C>A	GRCh38
NC_000001.10:g.227083139C>A , CM000663.1:g.227083139C>A	GRCh37
NC_000001.9:g.225149762C>A	NCBI36
NG_007381.1:g.29867C>A
NG_012825.2:g.2903C>A
NG_007381.2:g.30255C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1206C>A	ENSP00000355741.2:p.Thr402=
ENST00000366782.6:c.1206C>A	ENSP00000355746.2:p.Thr402=
ENST00000366783.8:c.1206C>A MANE Select	ENSP00000355747.3:p.Thr402=
ENST00000471728.2:n.1844C>A
ENST00000524196.6:c.1206C>A	ENSP00000429036.2:p.Thr402=
ENST00000626989.3:c.1206C>A	ENSP00000486498.2:p.Thr402=
ENST00000676467.1:c.*1033C>A	ENSP00000504294.1:n.*1033C>A
ENST00000676747.1:c.1188+1313C>A	ENSP00000503244.1:n.1188+1313C>A
ENST00000676884.1:c.1206C>A	ENSP00000503200.1:p.Thr402=
ENST00000676888.1:c.*547C>A	ENSP00000504483.1:n.*547C>A
ENST00000676907.1:c.*785C>A	ENSP00000504410.1:n.*785C>A
ENST00000676945.1:c.1191+1313C>A	ENSP00000504433.1:n.1191+1313C>A
ENST00000677065.1:n.1767C>A
ENST00000677414.1:c.1206C>A	ENSP00000503116.1:p.Thr402=
ENST00000677529.1:n.2936C>A
ENST00000677596.1:c.*1428C>A	ENSP00000503618.1:n.*1428C>A
ENST00000677599.1:c.1191+1313C>A	ENSP00000503673.1:n.1191+1313C>A
ENST00000677748.1:n.3461C>A
ENST00000677880.1:c.771C>A	ENSP00000503121.1:p.Thr257=
ENST00000678021.1:c.*829C>A	ENSP00000504674.1:n.*829C>A
ENST00000678233.1:c.1206C>A	ENSP00000504728.1:p.Thr402=
ENST00000678320.1:c.1107C>A	ENSP00000503680.1:p.Thr369=
ENST00000678655.1:c.1092+1313C>A	ENSP00000504230.1:n.1092+1313C>A
ENST00000678706.1:c.*583C>A	ENSP00000503659.1:n.*583C>A
ENST00000678776.1:c.*1343C>A	ENSP00000504624.1:n.*1343C>A
ENST00000678784.1:c.1073-2282C>A	ENSP00000504652.1:n.1073-2282C>A
ENST00000678820.1:c.1089+1313C>A	ENSP00000504138.1:n.1089+1313C>A
ENST00000678835.1:c.*757-2282C>A	ENSP00000504343.1:n.*757-2282C>A
ENST00000679088.1:c.1206C>A	ENSP00000504727.1:p.Thr402=
ENST00000679098.1:c.1206C>A	ENSP00000504303.1:p.Thr402=
ENST00000366782.5:c.1305C>A	ENSP00000355746.1:p.Thr435=
ENST00000366783.7:c.1206C>A	ENSP00000355747.3:p.Thr402=
ENST00000422240.6:c.1203C>A	ENSP00000403737.2:p.Thr401=
ENST00000471728.1:n.464C>A
ENST00000472139.2:c.774C>A	ENSP00000427806.1:p.Thr258=
ENST00000626989.2:c.1305C>A	ENSP00000486498.1:p.Thr435=
NM_000447.2:c.1206C>A	NP_000438.2:p.Thr402=
NM_012486.2:c.1203C>A	NP_036618.2:p.Thr401=
XM_005273199.2:c.1206C>A	XP_005273256.1:p.Thr402=
XM_011544236.1:c.774C>A	XP_011542538.1:p.Thr258=
XR_949149.1:n.1940C>A
XM_005273199.4:c.1206C>A	XP_005273256.1:p.Thr402=
XM_017001835.1:c.1206C>A	XP_016857324.1:p.Thr402=
XM_017001836.1:c.1203C>A	XP_016857325.1:p.Thr401=
XR_001737316.2:n.1478-2282C>A
XR_001737317.2:n.1478-2282C>A
XR_001737318.2:n.1921C>A
XR_001737319.1:n.2264C>A
XR_001737320.1:n.2261C>A
XR_001737321.1:n.1756C>A
XR_949149.2:n.1918C>A
XR_949150.3:n.2137C>A
NM_000447.3:c.1206C>A MANE Select	NP_000438.2:p.Thr402=
NM_012486.3:c.1203C>A	NP_036618.2:p.Thr401=