Canonical Allele Identifier: CA2698249563

Gene: PSEN2

Linked Data

• dbSNP Id: rs2102699305

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895661T>C , CM000663.2:g.226895661T>C	GRCh38
NC_000001.10:g.227083362T>C , CM000663.1:g.227083362T>C	GRCh37
NC_000001.9:g.225149985T>C	NCBI36
NG_007381.1:g.30090T>C
NG_012825.2:g.3126T>C
NG_007381.2:g.30478T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*82T>C	ENSP00000355741.2:n.*82T>C
ENST00000366782.6:c.*82T>C	ENSP00000355746.2:n.*82T>C
ENST00000366783.8:c.*82T>C MANE Select	ENSP00000355747.3:n.*82T>C
ENST00000471728.2:n.2067T>C
ENST00000524196.6:c.*82T>C	ENSP00000429036.2:n.*82T>C
ENST00000626989.3:c.*82T>C	ENSP00000486498.2:n.*82T>C
ENST00000676467.1:c.*1256T>C	ENSP00000504294.1:n.*1256T>C
ENST00000676747.1:c.1188+1536T>C	ENSP00000503244.1:n.1188+1536T>C
ENST00000676884.1:c.*82T>C	ENSP00000503200.1:n.*82T>C
ENST00000676888.1:c.*770T>C	ENSP00000504483.1:n.*770T>C
ENST00000676907.1:c.*1008T>C	ENSP00000504410.1:n.*1008T>C
ENST00000676945.1:c.1191+1536T>C	ENSP00000504433.1:n.1191+1536T>C
ENST00000677065.1:n.1990T>C
ENST00000677414.1:c.*82T>C	ENSP00000503116.1:n.*82T>C
ENST00000677529.1:n.3159T>C
ENST00000677596.1:c.*1651T>C	ENSP00000503618.1:n.*1651T>C
ENST00000677599.1:c.1191+1536T>C	ENSP00000503673.1:n.1191+1536T>C
ENST00000677748.1:n.3684T>C
ENST00000677880.1:c.*82T>C	ENSP00000503121.1:n.*82T>C
ENST00000678021.1:c.*1052T>C	ENSP00000504674.1:n.*1052T>C
ENST00000678233.1:c.*8+74T>C	ENSP00000504728.1:n.*8+74T>C
ENST00000678320.1:c.*82T>C	ENSP00000503680.1:n.*82T>C
ENST00000678655.1:c.1092+1536T>C	ENSP00000504230.1:n.1092+1536T>C
ENST00000678706.1:c.*806T>C	ENSP00000503659.1:n.*806T>C
ENST00000678776.1:c.*1566T>C	ENSP00000504624.1:n.*1566T>C
ENST00000678784.1:c.1073-2059T>C	ENSP00000504652.1:n.1073-2059T>C
ENST00000678820.1:c.1089+1536T>C	ENSP00000504138.1:n.1089+1536T>C
ENST00000678835.1:c.*757-2059T>C	ENSP00000504343.1:n.*757-2059T>C
ENST00000679088.1:c.*82T>C	ENSP00000504727.1:n.*82T>C
ENST00000679098.1:c.*8+74T>C	ENSP00000504303.1:n.*8+74T>C
ENST00000366782.5:c.*82T>C	ENSP00000355746.1:n.*82T>C
ENST00000366783.7:c.*82T>C	ENSP00000355747.3:n.*82T>C
ENST00000422240.6:c.*82T>C	ENSP00000403737.2:n.*82T>C
ENST00000472139.2:c.*82T>C	ENSP00000427806.1:n.*82T>C
ENST00000626989.2:c.1528T>C	ENSP00000486498.1:n.1528T>C
NM_000447.2:c.*82T>C	NP_000438.2:n.*82T>C
NM_012486.2:c.*82T>C	NP_036618.2:n.*82T>C
XM_005273199.2:c.*82T>C	XP_005273256.1:n.*82T>C
XM_011544236.1:c.*82T>C	XP_011542538.1:n.*82T>C
XM_005273199.4:c.*82T>C	XP_005273256.1:n.*82T>C
XM_017001835.1:c.*82T>C	XP_016857324.1:n.*82T>C
XM_017001836.1:c.*82T>C	XP_016857325.1:n.*82T>C
XR_001737316.2:n.1478-2059T>C
XR_001737317.2:n.1478-2059T>C
XR_001737318.2:n.2144T>C
XR_001737319.1:n.2487T>C
XR_001737320.1:n.2484T>C
XR_001737321.1:n.1979T>C
XR_949149.2:n.2141T>C
XR_949150.3:n.2360T>C
NM_000447.3:c.*82T>C MANE Select	NP_000438.2:n.*82T>C
NM_012486.3:c.*82T>C	NP_036618.2:n.*82T>C