Canonical Allele Identifier: CA1225082498

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226888963T= , CM000663.2:g.226888963T=	GRCh38
NC_000001.10:g.227076664T= , CM000663.1:g.227076664T=	GRCh37
NC_000001.9:g.225143287T=	NCBI36
NG_007381.1:g.23392T=
NG_007381.2:g.23780T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.701T=	ENSP00000355741.2:p.Met234=
ENST00000366782.6:c.701T=	ENSP00000355746.2:p.Met234=
ENST00000366783.8:c.701T= MANE Select	ENSP00000355747.3:p.Met234=
ENST00000524196.6:c.701T=	ENSP00000429036.2:p.Met234=
ENST00000626989.3:c.701T=	ENSP00000486498.2:p.Met234=
ENST00000676467.1:c.*531T=	ENSP00000504294.1:n.*531T=
ENST00000676747.1:c.701T=	ENSP00000503244.1:p.Met234=
ENST00000676840.1:c.701T=	ENSP00000504318.1:p.Met234=
ENST00000676884.1:c.701T=	ENSP00000503200.1:p.Met234=
ENST00000676888.1:c.701T=	ENSP00000504483.1:p.Met234=
ENST00000676907.1:c.*280T=	ENSP00000504410.1:n.*280T=
ENST00000676945.1:c.701T=	ENSP00000504433.1:p.Met234=
ENST00000677065.1:n.1262T=
ENST00000677414.1:c.701T=	ENSP00000503116.1:p.Met234=
ENST00000677529.1:n.1139T=
ENST00000677596.1:c.*608T=	ENSP00000503618.1:n.*608T=
ENST00000677599.1:c.701T=	ENSP00000503673.1:p.Met234=
ENST00000677748.1:n.1139T=
ENST00000677880.1:c.269T=	ENSP00000503121.1:p.Met90=
ENST00000678021.1:c.*324T=	ENSP00000504674.1:n.*324T=
ENST00000678233.1:c.701T=	ENSP00000504728.1:p.Met234=
ENST00000678320.1:c.701T=	ENSP00000503680.1:p.Met234=
ENST00000678655.1:c.701T=	ENSP00000504230.1:p.Met234=
ENST00000678706.1:c.701T=	ENSP00000503659.1:p.Met234=
ENST00000678776.1:c.*531T=	ENSP00000504624.1:n.*531T=
ENST00000678784.1:c.701T=	ENSP00000504652.1:p.Met234=
ENST00000678820.1:c.701T=	ENSP00000504138.1:p.Met234=
ENST00000678835.1:c.701T=	ENSP00000504343.1:p.Met234=
ENST00000679088.1:c.701T=	ENSP00000504727.1:p.Met234=
ENST00000679098.1:c.701T=	ENSP00000504303.1:p.Met234=
ENST00000366782.5:c.800T=	ENSP00000355746.1:p.Met267=
ENST00000366783.7:c.701T=	ENSP00000355747.3:p.Met234=
ENST00000422240.6:c.701T=	ENSP00000403737.2:p.Met234=
ENST00000460775.5:c.182T=	ENSP00000427912.1:p.Met61=
ENST00000472139.2:c.269T=	ENSP00000427806.1:p.Met90=
ENST00000626989.2:c.800T=	ENSP00000486498.1:p.Met267=
NM_000447.2:c.701T=	NP_000438.2:p.Met234=
NM_012486.2:c.701T=	NP_036618.2:p.Met234=
XM_005273199.2:c.701T=	XP_005273256.1:p.Met234=
XM_011544236.1:c.269T=	XP_011542538.1:p.Met90=
XR_949149.1:n.1128T=
XR_949150.1:n.1128T=
XM_005273199.4:c.701T=	XP_005273256.1:p.Met234=
XM_017001835.1:c.701T=	XP_016857324.1:p.Met234=
XM_017001836.1:c.701T=	XP_016857325.1:p.Met234=
XR_001737316.2:n.1106T=
XR_001737317.2:n.1106T=
XR_001737318.2:n.1106T=
XR_001737319.1:n.1449T=
XR_001737320.1:n.1449T=
XR_001737321.1:n.941T=
XR_949149.2:n.1106T=
XR_949150.3:n.1106T=
NM_000447.3:c.701T= MANE Select	NP_000438.2:p.Met234=
NM_012486.3:c.701T=	NP_036618.2:p.Met234=