Canonical Allele Identifier: CA345045107

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083191A>T (hg19) ; chr1:g.226895490A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895490A>T , CM000663.2:g.226895490A>T	GRCh38
NC_000001.10:g.227083191A>T , CM000663.1:g.227083191A>T	GRCh37
NC_000001.9:g.225149814A>T	NCBI36
NG_007381.1:g.29919A>T
NG_012825.2:g.2955A>T
NG_007381.2:g.30307A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1258A>T	ENSP00000355741.2:p.Ile420Phe
ENST00000366782.6:c.1258A>T	ENSP00000355746.2:p.Ile420Phe
ENST00000366783.8:c.1258A>T MANE Select	ENSP00000355747.3:p.Ile420Phe
ENST00000471728.2:n.1896A>T
ENST00000524196.6:c.1258A>T	ENSP00000429036.2:p.Ile420Phe
ENST00000626989.3:c.1258A>T	ENSP00000486498.2:p.Ile420Phe
ENST00000676467.1:c.*1085A>T	ENSP00000504294.1:n.*1085A>T
ENST00000676747.1:c.1188+1365A>T	ENSP00000503244.1:n.1188+1365A>T
ENST00000676884.1:c.1258A>T	ENSP00000503200.1:p.Ile420Phe
ENST00000676888.1:c.*599A>T	ENSP00000504483.1:n.*599A>T
ENST00000676907.1:c.*837A>T	ENSP00000504410.1:n.*837A>T
ENST00000676945.1:c.1191+1365A>T	ENSP00000504433.1:n.1191+1365A>T
ENST00000677065.1:n.1819A>T
ENST00000677414.1:c.1258A>T	ENSP00000503116.1:p.Ile420Phe
ENST00000677529.1:n.2988A>T
ENST00000677596.1:c.*1480A>T	ENSP00000503618.1:n.*1480A>T
ENST00000677599.1:c.1191+1365A>T	ENSP00000503673.1:n.1191+1365A>T
ENST00000677748.1:n.3513A>T
ENST00000677880.1:c.823A>T	ENSP00000503121.1:p.Ile275Phe
ENST00000678021.1:c.*881A>T	ENSP00000504674.1:n.*881A>T
ENST00000678233.1:c.1258A>T	ENSP00000504728.1:p.Ile420Phe
ENST00000678320.1:c.1159A>T	ENSP00000503680.1:p.Ile387Phe
ENST00000678655.1:c.1092+1365A>T	ENSP00000504230.1:n.1092+1365A>T
ENST00000678706.1:c.*635A>T	ENSP00000503659.1:n.*635A>T
ENST00000678776.1:c.*1395A>T	ENSP00000504624.1:n.*1395A>T
ENST00000678784.1:c.1073-2230A>T	ENSP00000504652.1:n.1073-2230A>T
ENST00000678820.1:c.1089+1365A>T	ENSP00000504138.1:n.1089+1365A>T
ENST00000678835.1:c.*757-2230A>T	ENSP00000504343.1:n.*757-2230A>T
ENST00000679088.1:c.1258A>T	ENSP00000504727.1:p.Ile420Phe
ENST00000679098.1:c.1258A>T	ENSP00000504303.1:p.Ile420Phe
ENST00000366782.5:c.1357A>T	ENSP00000355746.1:p.Ile453Phe
ENST00000366783.7:c.1258A>T	ENSP00000355747.3:p.Ile420Phe
ENST00000422240.6:c.1255A>T	ENSP00000403737.2:p.Ile419Phe
ENST00000471728.1:n.516A>T
ENST00000472139.2:c.826A>T	ENSP00000427806.1:p.Ile276Phe
ENST00000626989.2:c.1357A>T	ENSP00000486498.1:p.Ile453Phe
NM_000447.2:c.1258A>T	NP_000438.2:p.Ile420Phe
NM_012486.2:c.1255A>T	NP_036618.2:p.Ile419Phe
XM_005273199.2:c.1258A>T	XP_005273256.1:p.Ile420Phe
XM_011544236.1:c.826A>T	XP_011542538.1:p.Ile276Phe
XR_949149.1:n.1992A>T
XM_005273199.4:c.1258A>T	XP_005273256.1:p.Ile420Phe
XM_017001835.1:c.1258A>T	XP_016857324.1:p.Ile420Phe
XM_017001836.1:c.1255A>T	XP_016857325.1:p.Ile419Phe
XR_001737316.2:n.1478-2230A>T
XR_001737317.2:n.1478-2230A>T
XR_001737318.2:n.1973A>T
XR_001737319.1:n.2316A>T
XR_001737320.1:n.2313A>T
XR_001737321.1:n.1808A>T
XR_949149.2:n.1970A>T
XR_949150.3:n.2189A>T
NM_000447.3:c.1258A>T MANE Select	NP_000438.2:p.Ile420Phe
NM_012486.3:c.1255A>T	NP_036618.2:p.Ile419Phe