Canonical Allele Identifier: CA1225084659

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894113G= , CM000663.2:g.226894113G=	GRCh38
NC_000001.10:g.227081814G= , CM000663.1:g.227081814G=	GRCh37
NC_000001.9:g.225148437G=	NCBI36
NG_007381.1:g.28542G=
NG_012825.2:g.1578G=
NG_007381.2:g.28930G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1179G=	ENSP00000355741.2:p.Val393=
ENST00000366782.6:c.1179G=	ENSP00000355746.2:p.Val393=
ENST00000366783.8:c.1179G= MANE Select	ENSP00000355747.3:p.Val393=
ENST00000471728.2:n.1817G=
ENST00000524196.6:c.1179G=	ENSP00000429036.2:p.Val393=
ENST00000626989.3:c.1179G=	ENSP00000486498.2:p.Val393=
ENST00000676467.1:c.*1006G=	ENSP00000504294.1:n.*1006G=
ENST00000676747.1:c.1176G=	ENSP00000503244.1:p.Val392=
ENST00000676884.1:c.1179G=	ENSP00000503200.1:p.Val393=
ENST00000676888.1:c.*520G=	ENSP00000504483.1:n.*520G=
ENST00000676907.1:c.*758G=	ENSP00000504410.1:n.*758G=
ENST00000676945.1:c.1179G=	ENSP00000504433.1:p.Val393=
ENST00000677065.1:n.1740G=
ENST00000677414.1:c.1179G=	ENSP00000503116.1:p.Val393=
ENST00000677529.1:n.2909G=
ENST00000677596.1:c.*1401G=	ENSP00000503618.1:n.*1401G=
ENST00000677599.1:c.1179G=	ENSP00000503673.1:p.Val393=
ENST00000677748.1:n.3434G=
ENST00000677880.1:c.744G=	ENSP00000503121.1:p.Val248=
ENST00000678021.1:c.*802G=	ENSP00000504674.1:n.*802G=
ENST00000678233.1:c.1179G=	ENSP00000504728.1:p.Val393=
ENST00000678320.1:c.1080G=	ENSP00000503680.1:p.Val360=
ENST00000678655.1:c.1080G=	ENSP00000504230.1:p.Val360=
ENST00000678706.1:c.*556G=	ENSP00000503659.1:n.*556G=
ENST00000678776.1:c.*1316G=	ENSP00000504624.1:n.*1316G=
ENST00000678784.1:c.1072+2269G=	ENSP00000504652.1:n.1072+2269G=
ENST00000678820.1:c.1077G=	ENSP00000504138.1:p.Val359=
ENST00000678835.1:c.*756+2269G=	ENSP00000504343.1:n.*756+2269G=
ENST00000679088.1:c.1179G=	ENSP00000504727.1:p.Val393=
ENST00000679098.1:c.1179G=	ENSP00000504303.1:p.Val393=
ENST00000366782.5:c.1278G=	ENSP00000355746.1:p.Val426=
ENST00000366783.7:c.1179G=	ENSP00000355747.3:p.Val393=
ENST00000422240.6:c.1176G=	ENSP00000403737.2:p.Val392=
ENST00000471728.1:n.437G=
ENST00000472139.2:c.747G=	ENSP00000427806.1:p.Val249=
ENST00000626989.2:c.1278G=	ENSP00000486498.1:p.Val426=
NM_000447.2:c.1179G=	NP_000438.2:p.Val393=
NM_012486.2:c.1176G=	NP_036618.2:p.Val392=
XM_005273199.2:c.1179G=	XP_005273256.1:p.Val393=
XM_011544236.1:c.747G=	XP_011542538.1:p.Val249=
XR_949149.1:n.1913G=
XM_005273199.4:c.1179G=	XP_005273256.1:p.Val393=
XM_017001835.1:c.1179G=	XP_016857324.1:p.Val393=
XM_017001836.1:c.1176G=	XP_016857325.1:p.Val392=
XR_001737316.2:n.1477+2269G=
XR_001737317.2:n.1477+2269G=
XR_001737318.2:n.1894G=
XR_001737319.1:n.2237G=
XR_001737320.1:n.2234G=
XR_001737321.1:n.1729G=
XR_949149.2:n.1891G=
XR_949150.3:n.2110G=
NM_000447.3:c.1179G= MANE Select	NP_000438.2:p.Val393=
NM_012486.3:c.1176G=	NP_036618.2:p.Val392=