Canonical Allele Identifier: CA345043891

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227081711G>T (hg19) ; chr1:g.226894010G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894010G>T , CM000663.2:g.226894010G>T	GRCh38
NC_000001.10:g.227081711G>T , CM000663.1:g.227081711G>T	GRCh37
NC_000001.9:g.225148334G>T	NCBI36
NG_007381.1:g.28439G>T
NG_012825.2:g.1475G>T
NG_007381.2:g.28827G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1076G>T	ENSP00000355741.2:p.Gly359Val
ENST00000366782.6:c.1076G>T	ENSP00000355746.2:p.Gly359Val
ENST00000366783.8:c.1076G>T MANE Select	ENSP00000355747.3:p.Gly359Val
ENST00000471728.2:n.1714G>T
ENST00000524196.6:c.1076G>T	ENSP00000429036.2:p.Gly359Val
ENST00000626989.3:c.1076G>T	ENSP00000486498.2:p.Gly359Val
ENST00000676467.1:c.*903G>T	ENSP00000504294.1:n.*903G>T
ENST00000676747.1:c.1073G>T	ENSP00000503244.1:p.Gly358Val
ENST00000676884.1:c.1076G>T	ENSP00000503200.1:p.Gly359Val
ENST00000676888.1:c.*417G>T	ENSP00000504483.1:n.*417G>T
ENST00000676907.1:c.*655G>T	ENSP00000504410.1:n.*655G>T
ENST00000676945.1:c.1076G>T	ENSP00000504433.1:p.Gly359Val
ENST00000677065.1:n.1637G>T
ENST00000677414.1:c.1076G>T	ENSP00000503116.1:p.Gly359Val
ENST00000677529.1:n.2806G>T
ENST00000677596.1:c.*1298G>T	ENSP00000503618.1:n.*1298G>T
ENST00000677599.1:c.1076G>T	ENSP00000503673.1:p.Gly359Val
ENST00000677748.1:n.3331G>T
ENST00000677880.1:c.641G>T	ENSP00000503121.1:p.Gly214Val
ENST00000678021.1:c.*699G>T	ENSP00000504674.1:n.*699G>T
ENST00000678233.1:c.1076G>T	ENSP00000504728.1:p.Gly359Val
ENST00000678320.1:c.977G>T	ENSP00000503680.1:p.Gly326Val
ENST00000678655.1:c.977G>T	ENSP00000504230.1:p.Gly326Val
ENST00000678706.1:c.*453G>T	ENSP00000503659.1:n.*453G>T
ENST00000678776.1:c.*1213G>T	ENSP00000504624.1:n.*1213G>T
ENST00000678784.1:c.1072+2166G>T	ENSP00000504652.1:n.1072+2166G>T
ENST00000678820.1:c.974G>T	ENSP00000504138.1:p.Gly325Val
ENST00000678835.1:c.*756+2166G>T	ENSP00000504343.1:n.*756+2166G>T
ENST00000679088.1:c.1076G>T	ENSP00000504727.1:p.Gly359Val
ENST00000679098.1:c.1076G>T	ENSP00000504303.1:p.Gly359Val
ENST00000366782.5:c.1175G>T	ENSP00000355746.1:p.Gly392Val
ENST00000366783.7:c.1076G>T	ENSP00000355747.3:p.Gly359Val
ENST00000422240.6:c.1073G>T	ENSP00000403737.2:p.Gly358Val
ENST00000471728.1:n.334G>T
ENST00000472139.2:c.644G>T	ENSP00000427806.1:p.Gly215Val
ENST00000626989.2:c.1175G>T	ENSP00000486498.1:p.Gly392Val
NM_000447.2:c.1076G>T	NP_000438.2:p.Gly359Val
NM_012486.2:c.1073G>T	NP_036618.2:p.Gly358Val
XM_005273199.2:c.1076G>T	XP_005273256.1:p.Gly359Val
XM_011544236.1:c.644G>T	XP_011542538.1:p.Gly215Val
XR_949149.1:n.1810G>T
XM_005273199.4:c.1076G>T	XP_005273256.1:p.Gly359Val
XM_017001835.1:c.1076G>T	XP_016857324.1:p.Gly359Val
XM_017001836.1:c.1073G>T	XP_016857325.1:p.Gly358Val
XR_001737316.2:n.1477+2166G>T
XR_001737317.2:n.1477+2166G>T
XR_001737318.2:n.1791G>T
XR_001737319.1:n.2134G>T
XR_001737320.1:n.2131G>T
XR_001737321.1:n.1626G>T
XR_949149.2:n.1788G>T
XR_949150.3:n.2007G>T
NM_000447.3:c.1076G>T MANE Select	NP_000438.2:p.Gly359Val
NM_012486.3:c.1073G>T	NP_036618.2:p.Gly358Val