Canonical Allele Identifier: CA1225082466

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226888857A= , CM000663.2:g.226888857A=	GRCh38
NC_000001.10:g.227076558A= , CM000663.1:g.227076558A=	GRCh37
NC_000001.9:g.225143181A=	NCBI36
NG_007381.1:g.23286A=
NG_007381.2:g.23674A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.595A=	ENSP00000355741.2:p.Met199=
ENST00000366782.6:c.595A=	ENSP00000355746.2:p.Met199=
ENST00000366783.8:c.595A= MANE Select	ENSP00000355747.3:p.Met199=
ENST00000524196.6:c.595A=	ENSP00000429036.2:p.Met199=
ENST00000626989.3:c.595A=	ENSP00000486498.2:p.Met199=
ENST00000676467.1:c.*425A=	ENSP00000504294.1:n.*425A=
ENST00000676747.1:c.595A=	ENSP00000503244.1:p.Met199=
ENST00000676840.1:c.595A=	ENSP00000504318.1:p.Met199=
ENST00000676884.1:c.595A=	ENSP00000503200.1:p.Met199=
ENST00000676888.1:c.595A=	ENSP00000504483.1:p.Met199=
ENST00000676907.1:c.*174A=	ENSP00000504410.1:n.*174A=
ENST00000676945.1:c.595A=	ENSP00000504433.1:p.Met199=
ENST00000677065.1:n.1156A=
ENST00000677414.1:c.595A=	ENSP00000503116.1:p.Met199=
ENST00000677529.1:n.1033A=
ENST00000677596.1:c.*502A=	ENSP00000503618.1:n.*502A=
ENST00000677599.1:c.595A=	ENSP00000503673.1:p.Met199=
ENST00000677748.1:n.1033A=
ENST00000677880.1:c.163A=	ENSP00000503121.1:p.Met55=
ENST00000678021.1:c.*218A=	ENSP00000504674.1:n.*218A=
ENST00000678233.1:c.595A=	ENSP00000504728.1:p.Met199=
ENST00000678320.1:c.595A=	ENSP00000503680.1:p.Met199=
ENST00000678655.1:c.595A=	ENSP00000504230.1:p.Met199=
ENST00000678706.1:c.595A=	ENSP00000503659.1:p.Met199=
ENST00000678776.1:c.*425A=	ENSP00000504624.1:n.*425A=
ENST00000678784.1:c.595A=	ENSP00000504652.1:p.Met199=
ENST00000678820.1:c.595A=	ENSP00000504138.1:p.Met199=
ENST00000678835.1:c.595A=	ENSP00000504343.1:p.Met199=
ENST00000679088.1:c.595A=	ENSP00000504727.1:p.Met199=
ENST00000679098.1:c.595A=	ENSP00000504303.1:p.Met199=
ENST00000366782.5:c.694A=	ENSP00000355746.1:p.Met232=
ENST00000366783.7:c.595A=	ENSP00000355747.3:p.Met199=
ENST00000422240.6:c.595A=	ENSP00000403737.2:p.Met199=
ENST00000460775.5:c.76A=	ENSP00000427912.1:p.Met26=
ENST00000472139.2:c.163A=	ENSP00000427806.1:p.Met55=
ENST00000626989.2:c.694A=	ENSP00000486498.1:p.Met232=
NM_000447.2:c.595A=	NP_000438.2:p.Met199=
NM_012486.2:c.595A=	NP_036618.2:p.Met199=
XM_005273199.2:c.595A=	XP_005273256.1:p.Met199=
XM_011544236.1:c.163A=	XP_011542538.1:p.Met55=
XR_949149.1:n.1022A=
XR_949150.1:n.1022A=
XM_005273199.4:c.595A=	XP_005273256.1:p.Met199=
XM_017001835.1:c.595A=	XP_016857324.1:p.Met199=
XM_017001836.1:c.595A=	XP_016857325.1:p.Met199=
XR_001737316.2:n.1000A=
XR_001737317.2:n.1000A=
XR_001737318.2:n.1000A=
XR_001737319.1:n.1343A=
XR_001737320.1:n.1343A=
XR_001737321.1:n.835A=
XR_949149.2:n.1000A=
XR_949150.3:n.1000A=
NM_000447.3:c.595A= MANE Select	NP_000438.2:p.Met199=
NM_012486.3:c.595A=	NP_036618.2:p.Met199=