Canonical Allele Identifier: CA345045250

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083209T>C (hg19) ; chr1:g.226895508T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895508T>C , CM000663.2:g.226895508T>C	GRCh38
NC_000001.10:g.227083209T>C , CM000663.1:g.227083209T>C	GRCh37
NC_000001.9:g.225149832T>C	NCBI36
NG_007381.1:g.29937T>C
NG_012825.2:g.2973T>C
NG_007381.2:g.30325T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1276T>C	ENSP00000355741.2:p.Phe426Leu
ENST00000366782.6:c.1276T>C	ENSP00000355746.2:p.Phe426Leu
ENST00000366783.8:c.1276T>C MANE Select	ENSP00000355747.3:p.Phe426Leu
ENST00000471728.2:n.1914T>C
ENST00000524196.6:c.1276T>C	ENSP00000429036.2:p.Phe426Leu
ENST00000626989.3:c.1276T>C	ENSP00000486498.2:p.Phe426Leu
ENST00000676467.1:c.*1103T>C	ENSP00000504294.1:n.*1103T>C
ENST00000676747.1:c.1188+1383T>C	ENSP00000503244.1:n.1188+1383T>C
ENST00000676884.1:c.1276T>C	ENSP00000503200.1:p.Phe426Leu
ENST00000676888.1:c.*617T>C	ENSP00000504483.1:n.*617T>C
ENST00000676907.1:c.*855T>C	ENSP00000504410.1:n.*855T>C
ENST00000676945.1:c.1191+1383T>C	ENSP00000504433.1:n.1191+1383T>C
ENST00000677065.1:n.1837T>C
ENST00000677414.1:c.1276T>C	ENSP00000503116.1:p.Phe426Leu
ENST00000677529.1:n.3006T>C
ENST00000677596.1:c.*1498T>C	ENSP00000503618.1:n.*1498T>C
ENST00000677599.1:c.1191+1383T>C	ENSP00000503673.1:n.1191+1383T>C
ENST00000677748.1:n.3531T>C
ENST00000677880.1:c.841T>C	ENSP00000503121.1:p.Phe281Leu
ENST00000678021.1:c.*899T>C	ENSP00000504674.1:n.*899T>C
ENST00000678233.1:c.1276T>C	ENSP00000504728.1:p.Phe426Leu
ENST00000678320.1:c.1177T>C	ENSP00000503680.1:p.Phe393Leu
ENST00000678655.1:c.1092+1383T>C	ENSP00000504230.1:n.1092+1383T>C
ENST00000678706.1:c.*653T>C	ENSP00000503659.1:n.*653T>C
ENST00000678776.1:c.*1413T>C	ENSP00000504624.1:n.*1413T>C
ENST00000678784.1:c.1073-2212T>C	ENSP00000504652.1:n.1073-2212T>C
ENST00000678820.1:c.1089+1383T>C	ENSP00000504138.1:n.1089+1383T>C
ENST00000678835.1:c.*757-2212T>C	ENSP00000504343.1:n.*757-2212T>C
ENST00000679088.1:c.1276T>C	ENSP00000504727.1:p.Phe426Leu
ENST00000679098.1:c.1276T>C	ENSP00000504303.1:p.Phe426Leu
ENST00000366782.5:c.1375T>C	ENSP00000355746.1:p.Phe459Leu
ENST00000366783.7:c.1276T>C	ENSP00000355747.3:p.Phe426Leu
ENST00000422240.6:c.1273T>C	ENSP00000403737.2:p.Phe425Leu
ENST00000471728.1:n.534T>C
ENST00000472139.2:c.844T>C	ENSP00000427806.1:p.Phe282Leu
ENST00000626989.2:c.1375T>C	ENSP00000486498.1:p.Phe459Leu
NM_000447.2:c.1276T>C	NP_000438.2:p.Phe426Leu
NM_012486.2:c.1273T>C	NP_036618.2:p.Phe425Leu
XM_005273199.2:c.1276T>C	XP_005273256.1:p.Phe426Leu
XM_011544236.1:c.844T>C	XP_011542538.1:p.Phe282Leu
XR_949149.1:n.2010T>C
XM_005273199.4:c.1276T>C	XP_005273256.1:p.Phe426Leu
XM_017001835.1:c.1276T>C	XP_016857324.1:p.Phe426Leu
XM_017001836.1:c.1273T>C	XP_016857325.1:p.Phe425Leu
XR_001737316.2:n.1478-2212T>C
XR_001737317.2:n.1478-2212T>C
XR_001737318.2:n.1991T>C
XR_001737319.1:n.2334T>C
XR_001737320.1:n.2331T>C
XR_001737321.1:n.1826T>C
XR_949149.2:n.1988T>C
XR_949150.3:n.2207T>C
NM_000447.3:c.1276T>C MANE Select	NP_000438.2:p.Phe426Leu
NM_012486.3:c.1273T>C	NP_036618.2:p.Phe425Leu