Canonical Allele Identifier: CA38625161

Gene: PSEN2

Linked Data

• dbSNP Id: rs940775081
• gnomAD v4: 1-226894007-G-C
• MyVariant Identifiers: chr1:g.227081708G>C (hg19) ; chr1:g.226894007G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894007G>C , CM000663.2:g.226894007G>C	GRCh38
NC_000001.10:g.227081708G>C , CM000663.1:g.227081708G>C	GRCh37
NC_000001.9:g.225148331G>C	NCBI36
NG_007381.1:g.28436G>C
NG_012825.2:g.1472G>C
NG_007381.2:g.28824G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1073G>C	ENSP00000355741.2:p.Arg358Thr
ENST00000366782.6:c.1073G>C	ENSP00000355746.2:p.Arg358Thr
ENST00000366783.8:c.1073G>C MANE Select	ENSP00000355747.3:p.Arg358Thr
ENST00000471728.2:n.1711G>C
ENST00000524196.6:c.1073G>C	ENSP00000429036.2:p.Arg358Thr
ENST00000626989.3:c.1073G>C	ENSP00000486498.2:p.Arg358Thr
ENST00000676467.1:c.*900G>C	ENSP00000504294.1:n.*900G>C
ENST00000676747.1:c.1070G>C	ENSP00000503244.1:p.Arg357Thr
ENST00000676884.1:c.1073G>C	ENSP00000503200.1:p.Arg358Thr
ENST00000676888.1:c.*414G>C	ENSP00000504483.1:n.*414G>C
ENST00000676907.1:c.*652G>C	ENSP00000504410.1:n.*652G>C
ENST00000676945.1:c.1073G>C	ENSP00000504433.1:p.Arg358Thr
ENST00000677065.1:n.1634G>C
ENST00000677414.1:c.1073G>C	ENSP00000503116.1:p.Arg358Thr
ENST00000677529.1:n.2803G>C
ENST00000677596.1:c.*1295G>C	ENSP00000503618.1:n.*1295G>C
ENST00000677599.1:c.1073G>C	ENSP00000503673.1:p.Arg358Thr
ENST00000677748.1:n.3328G>C
ENST00000677880.1:c.638G>C	ENSP00000503121.1:p.Arg213Thr
ENST00000678021.1:c.*696G>C	ENSP00000504674.1:n.*696G>C
ENST00000678233.1:c.1073G>C	ENSP00000504728.1:p.Arg358Thr
ENST00000678320.1:c.974G>C	ENSP00000503680.1:p.Arg325Thr
ENST00000678655.1:c.974G>C	ENSP00000504230.1:p.Arg325Thr
ENST00000678706.1:c.*450G>C	ENSP00000503659.1:n.*450G>C
ENST00000678776.1:c.*1210G>C	ENSP00000504624.1:n.*1210G>C
ENST00000678784.1:c.1072+2163G>C	ENSP00000504652.1:n.1072+2163G>C
ENST00000678820.1:c.971G>C	ENSP00000504138.1:p.Arg324Thr
ENST00000678835.1:c.*756+2163G>C	ENSP00000504343.1:n.*756+2163G>C
ENST00000679088.1:c.1073G>C	ENSP00000504727.1:p.Arg358Thr
ENST00000679098.1:c.1073G>C	ENSP00000504303.1:p.Arg358Thr
ENST00000366782.5:c.1172G>C	ENSP00000355746.1:p.Arg391Thr
ENST00000366783.7:c.1073G>C	ENSP00000355747.3:p.Arg358Thr
ENST00000422240.6:c.1070G>C	ENSP00000403737.2:p.Arg357Thr
ENST00000471728.1:n.331G>C
ENST00000472139.2:c.641G>C	ENSP00000427806.1:p.Arg214Thr
ENST00000626989.2:c.1172G>C	ENSP00000486498.1:p.Arg391Thr
NM_000447.2:c.1073G>C	NP_000438.2:p.Arg358Thr
NM_012486.2:c.1070G>C	NP_036618.2:p.Arg357Thr
XM_005273199.2:c.1073G>C	XP_005273256.1:p.Arg358Thr
XM_011544236.1:c.641G>C	XP_011542538.1:p.Arg214Thr
XR_949149.1:n.1807G>C
XM_005273199.4:c.1073G>C	XP_005273256.1:p.Arg358Thr
XM_017001835.1:c.1073G>C	XP_016857324.1:p.Arg358Thr
XM_017001836.1:c.1070G>C	XP_016857325.1:p.Arg357Thr
XR_001737316.2:n.1477+2163G>C
XR_001737317.2:n.1477+2163G>C
XR_001737318.2:n.1788G>C
XR_001737319.1:n.2131G>C
XR_001737320.1:n.2128G>C
XR_001737321.1:n.1623G>C
XR_949149.2:n.1785G>C
XR_949150.3:n.2004G>C
NM_000447.3:c.1073G>C MANE Select	NP_000438.2:p.Arg358Thr
NM_012486.3:c.1070G>C	NP_036618.2:p.Arg357Thr