Canonical Allele Identifier: CA1225085332

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895612G= , CM000663.2:g.226895612G=	GRCh38
NC_000001.10:g.227083313G= , CM000663.1:g.227083313G=	GRCh37
NC_000001.9:g.225149936G=	NCBI36
NG_007381.1:g.30041G=
NG_012825.2:g.3077G=
NG_007381.2:g.30429G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*33G=	ENSP00000355741.2:n.*33G=
ENST00000366782.6:c.*33G=	ENSP00000355746.2:n.*33G=
ENST00000366783.8:c.*33G= MANE Select	ENSP00000355747.3:n.*33G=
ENST00000471728.2:n.2018G=
ENST00000524196.6:c.*33G=	ENSP00000429036.2:n.*33G=
ENST00000626989.3:c.*33G=	ENSP00000486498.2:n.*33G=
ENST00000676467.1:c.*1207G=	ENSP00000504294.1:n.*1207G=
ENST00000676747.1:c.1188+1487G=	ENSP00000503244.1:n.1188+1487G=
ENST00000676884.1:c.*33G=	ENSP00000503200.1:n.*33G=
ENST00000676888.1:c.*721G=	ENSP00000504483.1:n.*721G=
ENST00000676907.1:c.*959G=	ENSP00000504410.1:n.*959G=
ENST00000676945.1:c.1191+1487G=	ENSP00000504433.1:n.1191+1487G=
ENST00000677065.1:n.1941G=
ENST00000677414.1:c.*33G=	ENSP00000503116.1:n.*33G=
ENST00000677529.1:n.3110G=
ENST00000677596.1:c.*1602G=	ENSP00000503618.1:n.*1602G=
ENST00000677599.1:c.1191+1487G=	ENSP00000503673.1:n.1191+1487G=
ENST00000677748.1:n.3635G=
ENST00000677880.1:c.*33G=	ENSP00000503121.1:n.*33G=
ENST00000678021.1:c.*1003G=	ENSP00000504674.1:n.*1003G=
ENST00000678233.1:c.*8+25G=	ENSP00000504728.1:n.*8+25G=
ENST00000678320.1:c.*33G=	ENSP00000503680.1:n.*33G=
ENST00000678655.1:c.1092+1487G=	ENSP00000504230.1:n.1092+1487G=
ENST00000678706.1:c.*757G=	ENSP00000503659.1:n.*757G=
ENST00000678776.1:c.*1517G=	ENSP00000504624.1:n.*1517G=
ENST00000678784.1:c.1073-2108G=	ENSP00000504652.1:n.1073-2108G=
ENST00000678820.1:c.1089+1487G=	ENSP00000504138.1:n.1089+1487G=
ENST00000678835.1:c.*757-2108G=	ENSP00000504343.1:n.*757-2108G=
ENST00000679088.1:c.*33G=	ENSP00000504727.1:n.*33G=
ENST00000679098.1:c.*8+25G=	ENSP00000504303.1:n.*8+25G=
ENST00000366782.5:c.*33G=	ENSP00000355746.1:n.*33G=
ENST00000366783.7:c.*33G=	ENSP00000355747.3:n.*33G=
ENST00000422240.6:c.*33G=	ENSP00000403737.2:n.*33G=
ENST00000472139.2:c.*33G=	ENSP00000427806.1:n.*33G=
ENST00000626989.2:c.1479G=	ENSP00000486498.1:n.1479G=
NM_000447.2:c.*33G=	NP_000438.2:n.*33G=
NM_012486.2:c.*33G=	NP_036618.2:n.*33G=
XM_005273199.2:c.*33G=	XP_005273256.1:n.*33G=
XM_011544236.1:c.*33G=	XP_011542538.1:n.*33G=
XM_005273199.4:c.*33G=	XP_005273256.1:n.*33G=
XM_017001835.1:c.*33G=	XP_016857324.1:n.*33G=
XM_017001836.1:c.*33G=	XP_016857325.1:n.*33G=
XR_001737316.2:n.1478-2108G=
XR_001737317.2:n.1478-2108G=
XR_001737318.2:n.2095G=
XR_001737319.1:n.2438G=
XR_001737320.1:n.2435G=
XR_001737321.1:n.1930G=
XR_949149.2:n.2092G=
XR_949150.3:n.2311G=
NM_000447.3:c.*33G= MANE Select	NP_000438.2:n.*33G=
NM_012486.3:c.*33G=	NP_036618.2:n.*33G=