Canonical Allele Identifier: CA1146073767

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226893826C= , CM000663.2:g.226893826C=	GRCh38
NC_000001.10:g.227081527C= , CM000663.1:g.227081527C=	GRCh37
NC_000001.9:g.225148150C=	NCBI36
NG_007381.1:g.28255C=
NG_012825.2:g.1291C=
NG_007381.2:g.28643C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1073-181C=	ENSP00000355741.2:n.1073-181C=
ENST00000366782.6:c.1073-181C=	ENSP00000355746.2:n.1073-181C=
ENST00000366783.8:c.1073-181C= MANE Select	ENSP00000355747.3:n.1073-181C=
ENST00000471728.2:n.1711-181C=
ENST00000524196.6:c.1073-181C=	ENSP00000429036.2:n.1073-181C=
ENST00000626989.3:c.1073-181C=	ENSP00000486498.2:n.1073-181C=
ENST00000676467.1:c.*900-181C=	ENSP00000504294.1:n.*900-181C=
ENST00000676747.1:c.1070-181C=	ENSP00000503244.1:n.1070-181C=
ENST00000676884.1:c.1073-181C=	ENSP00000503200.1:n.1073-181C=
ENST00000676888.1:c.*414-181C=	ENSP00000504483.1:n.*414-181C=
ENST00000676907.1:c.*652-181C=	ENSP00000504410.1:n.*652-181C=
ENST00000676945.1:c.1073-181C=	ENSP00000504433.1:n.1073-181C=
ENST00000677065.1:n.1634-181C=
ENST00000677414.1:c.1073-181C=	ENSP00000503116.1:n.1073-181C=
ENST00000677529.1:n.2803-181C=
ENST00000677596.1:c.*1295-181C=	ENSP00000503618.1:n.*1295-181C=
ENST00000677599.1:c.1073-181C=	ENSP00000503673.1:n.1073-181C=
ENST00000677748.1:n.3328-181C=
ENST00000677880.1:c.638-181C=	ENSP00000503121.1:n.638-181C=
ENST00000678021.1:c.*696-181C=	ENSP00000504674.1:n.*696-181C=
ENST00000678233.1:c.1073-181C=	ENSP00000504728.1:n.1073-181C=
ENST00000678320.1:c.974-181C=	ENSP00000503680.1:n.974-181C=
ENST00000678655.1:c.974-181C=	ENSP00000504230.1:n.974-181C=
ENST00000678706.1:c.*450-181C=	ENSP00000503659.1:n.*450-181C=
ENST00000678776.1:c.*1210-181C=	ENSP00000504624.1:n.*1210-181C=
ENST00000678784.1:c.1072+1982C=	ENSP00000504652.1:n.1072+1982C=
ENST00000678820.1:c.971-181C=	ENSP00000504138.1:n.971-181C=
ENST00000678835.1:c.*756+1982C=	ENSP00000504343.1:n.*756+1982C=
ENST00000679088.1:c.1073-181C=	ENSP00000504727.1:n.1073-181C=
ENST00000679098.1:c.1073-181C=	ENSP00000504303.1:n.1073-181C=
ENST00000366782.5:c.1172-181C=	ENSP00000355746.1:n.1172-181C=
ENST00000366783.7:c.1073-181C=	ENSP00000355747.3:n.1073-181C=
ENST00000422240.6:c.1070-181C=	ENSP00000403737.2:n.1070-181C=
ENST00000471728.1:n.331-181C=
ENST00000472139.2:c.641-181C=	ENSP00000427806.1:n.641-181C=
ENST00000626989.2:c.1172-181C=	ENSP00000486498.1:n.1172-181C=
NM_000447.2:c.1073-181C=	NP_000438.2:n.1073-181C=
NM_012486.2:c.1070-181C=	NP_036618.2:n.1070-181C=
XM_005273199.2:c.1073-181C=	XP_005273256.1:n.1073-181C=
XM_011544236.1:c.641-181C=	XP_011542538.1:n.641-181C=
XR_949149.1:n.1807-181C=
XM_005273199.4:c.1073-181C=	XP_005273256.1:n.1073-181C=
XM_017001835.1:c.1073-181C=	XP_016857324.1:n.1073-181C=
XM_017001836.1:c.1070-181C=	XP_016857325.1:n.1070-181C=
XR_001737316.2:n.1477+1982C=
XR_001737317.2:n.1477+1982C=
XR_001737318.2:n.1788-181C=
XR_001737319.1:n.2131-181C=
XR_001737320.1:n.2128-181C=
XR_001737321.1:n.1623-181C=
XR_949149.2:n.1785-181C=
XR_949150.3:n.2004-181C=
NM_000447.3:c.1073-181C= MANE Select	NP_000438.2:n.1073-181C=
NM_012486.3:c.1070-181C=	NP_036618.2:n.1070-181C=