Canonical Allele Identifier: CA1225085276

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895467C= , CM000663.2:g.226895467C=	GRCh38
NC_000001.10:g.227083168C= , CM000663.1:g.227083168C=	GRCh37
NC_000001.9:g.225149791C=	NCBI36
NG_007381.1:g.29896C=
NG_012825.2:g.2932C=
NG_007381.2:g.30284C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1235C=	ENSP00000355741.2:p.Ala412=
ENST00000366782.6:c.1235C=	ENSP00000355746.2:p.Ala412=
ENST00000366783.8:c.1235C= MANE Select	ENSP00000355747.3:p.Ala412=
ENST00000471728.2:n.1873C=
ENST00000524196.6:c.1235C=	ENSP00000429036.2:p.Ala412=
ENST00000626989.3:c.1235C=	ENSP00000486498.2:p.Ala412=
ENST00000676467.1:c.*1062C=	ENSP00000504294.1:n.*1062C=
ENST00000676747.1:c.1188+1342C=	ENSP00000503244.1:n.1188+1342C=
ENST00000676884.1:c.1235C=	ENSP00000503200.1:p.Ala412=
ENST00000676888.1:c.*576C=	ENSP00000504483.1:n.*576C=
ENST00000676907.1:c.*814C=	ENSP00000504410.1:n.*814C=
ENST00000676945.1:c.1191+1342C=	ENSP00000504433.1:n.1191+1342C=
ENST00000677065.1:n.1796C=
ENST00000677414.1:c.1235C=	ENSP00000503116.1:p.Ala412=
ENST00000677529.1:n.2965C=
ENST00000677596.1:c.*1457C=	ENSP00000503618.1:n.*1457C=
ENST00000677599.1:c.1191+1342C=	ENSP00000503673.1:n.1191+1342C=
ENST00000677748.1:n.3490C=
ENST00000677880.1:c.800C=	ENSP00000503121.1:p.Ala267=
ENST00000678021.1:c.*858C=	ENSP00000504674.1:n.*858C=
ENST00000678233.1:c.1235C=	ENSP00000504728.1:p.Ala412=
ENST00000678320.1:c.1136C=	ENSP00000503680.1:p.Ala379=
ENST00000678655.1:c.1092+1342C=	ENSP00000504230.1:n.1092+1342C=
ENST00000678706.1:c.*612C=	ENSP00000503659.1:n.*612C=
ENST00000678776.1:c.*1372C=	ENSP00000504624.1:n.*1372C=
ENST00000678784.1:c.1073-2253C=	ENSP00000504652.1:n.1073-2253C=
ENST00000678820.1:c.1089+1342C=	ENSP00000504138.1:n.1089+1342C=
ENST00000678835.1:c.*757-2253C=	ENSP00000504343.1:n.*757-2253C=
ENST00000679088.1:c.1235C=	ENSP00000504727.1:p.Ala412=
ENST00000679098.1:c.1235C=	ENSP00000504303.1:p.Ala412=
ENST00000366782.5:c.1334C=	ENSP00000355746.1:p.Ala445=
ENST00000366783.7:c.1235C=	ENSP00000355747.3:p.Ala412=
ENST00000422240.6:c.1232C=	ENSP00000403737.2:p.Ala411=
ENST00000471728.1:n.493C=
ENST00000472139.2:c.803C=	ENSP00000427806.1:p.Ala268=
ENST00000626989.2:c.1334C=	ENSP00000486498.1:p.Ala445=
NM_000447.2:c.1235C=	NP_000438.2:p.Ala412=
NM_012486.2:c.1232C=	NP_036618.2:p.Ala411=
XM_005273199.2:c.1235C=	XP_005273256.1:p.Ala412=
XM_011544236.1:c.803C=	XP_011542538.1:p.Ala268=
XR_949149.1:n.1969C=
XM_005273199.4:c.1235C=	XP_005273256.1:p.Ala412=
XM_017001835.1:c.1235C=	XP_016857324.1:p.Ala412=
XM_017001836.1:c.1232C=	XP_016857325.1:p.Ala411=
XR_001737316.2:n.1478-2253C=
XR_001737317.2:n.1478-2253C=
XR_001737318.2:n.1950C=
XR_001737319.1:n.2293C=
XR_001737320.1:n.2290C=
XR_001737321.1:n.1785C=
XR_949149.2:n.1947C=
XR_949150.3:n.2166C=
NM_000447.3:c.1235C= MANE Select	NP_000438.2:p.Ala412=
NM_012486.3:c.1232C=	NP_036618.2:p.Ala411=