Canonical Allele Identifier: CA345043929

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227081729G>T (hg19) ; chr1:g.226894028G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894028G>T , CM000663.2:g.226894028G>T	GRCh38
NC_000001.10:g.227081729G>T , CM000663.1:g.227081729G>T	GRCh37
NC_000001.9:g.225148352G>T	NCBI36
NG_007381.1:g.28457G>T
NG_012825.2:g.1493G>T
NG_007381.2:g.28845G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1094G>T	ENSP00000355741.2:p.Gly365Val
ENST00000366782.6:c.1094G>T	ENSP00000355746.2:p.Gly365Val
ENST00000366783.8:c.1094G>T MANE Select	ENSP00000355747.3:p.Gly365Val
ENST00000471728.2:n.1732G>T
ENST00000524196.6:c.1094G>T	ENSP00000429036.2:p.Gly365Val
ENST00000626989.3:c.1094G>T	ENSP00000486498.2:p.Gly365Val
ENST00000676467.1:c.*921G>T	ENSP00000504294.1:n.*921G>T
ENST00000676747.1:c.1091G>T	ENSP00000503244.1:p.Gly364Val
ENST00000676884.1:c.1094G>T	ENSP00000503200.1:p.Gly365Val
ENST00000676888.1:c.*435G>T	ENSP00000504483.1:n.*435G>T
ENST00000676907.1:c.*673G>T	ENSP00000504410.1:n.*673G>T
ENST00000676945.1:c.1094G>T	ENSP00000504433.1:p.Gly365Val
ENST00000677065.1:n.1655G>T
ENST00000677414.1:c.1094G>T	ENSP00000503116.1:p.Gly365Val
ENST00000677529.1:n.2824G>T
ENST00000677596.1:c.*1316G>T	ENSP00000503618.1:n.*1316G>T
ENST00000677599.1:c.1094G>T	ENSP00000503673.1:p.Gly365Val
ENST00000677748.1:n.3349G>T
ENST00000677880.1:c.659G>T	ENSP00000503121.1:p.Gly220Val
ENST00000678021.1:c.*717G>T	ENSP00000504674.1:n.*717G>T
ENST00000678233.1:c.1094G>T	ENSP00000504728.1:p.Gly365Val
ENST00000678320.1:c.995G>T	ENSP00000503680.1:p.Gly332Val
ENST00000678655.1:c.995G>T	ENSP00000504230.1:p.Gly332Val
ENST00000678706.1:c.*471G>T	ENSP00000503659.1:n.*471G>T
ENST00000678776.1:c.*1231G>T	ENSP00000504624.1:n.*1231G>T
ENST00000678784.1:c.1072+2184G>T	ENSP00000504652.1:n.1072+2184G>T
ENST00000678820.1:c.992G>T	ENSP00000504138.1:p.Gly331Val
ENST00000678835.1:c.*756+2184G>T	ENSP00000504343.1:n.*756+2184G>T
ENST00000679088.1:c.1094G>T	ENSP00000504727.1:p.Gly365Val
ENST00000679098.1:c.1094G>T	ENSP00000504303.1:p.Gly365Val
ENST00000366782.5:c.1193G>T	ENSP00000355746.1:p.Gly398Val
ENST00000366783.7:c.1094G>T	ENSP00000355747.3:p.Gly365Val
ENST00000422240.6:c.1091G>T	ENSP00000403737.2:p.Gly364Val
ENST00000471728.1:n.352G>T
ENST00000472139.2:c.662G>T	ENSP00000427806.1:p.Gly221Val
ENST00000626989.2:c.1193G>T	ENSP00000486498.1:p.Gly398Val
NM_000447.2:c.1094G>T	NP_000438.2:p.Gly365Val
NM_012486.2:c.1091G>T	NP_036618.2:p.Gly364Val
XM_005273199.2:c.1094G>T	XP_005273256.1:p.Gly365Val
XM_011544236.1:c.662G>T	XP_011542538.1:p.Gly221Val
XR_949149.1:n.1828G>T
XM_005273199.4:c.1094G>T	XP_005273256.1:p.Gly365Val
XM_017001835.1:c.1094G>T	XP_016857324.1:p.Gly365Val
XM_017001836.1:c.1091G>T	XP_016857325.1:p.Gly364Val
XR_001737316.2:n.1477+2184G>T
XR_001737317.2:n.1477+2184G>T
XR_001737318.2:n.1809G>T
XR_001737319.1:n.2152G>T
XR_001737320.1:n.2149G>T
XR_001737321.1:n.1644G>T
XR_949149.2:n.1806G>T
XR_949150.3:n.2025G>T
NM_000447.3:c.1094G>T MANE Select	NP_000438.2:p.Gly365Val
NM_012486.3:c.1091G>T	NP_036618.2:p.Gly364Val