Canonical Allele Identifier: CA345043909

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227081720T>G (hg19) ; chr1:g.226894019T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894019T>G , CM000663.2:g.226894019T>G	GRCh38
NC_000001.10:g.227081720T>G , CM000663.1:g.227081720T>G	GRCh37
NC_000001.9:g.225148343T>G	NCBI36
NG_007381.1:g.28448T>G
NG_012825.2:g.1484T>G
NG_007381.2:g.28836T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1085T>G	ENSP00000355741.2:p.Leu362Arg
ENST00000366782.6:c.1085T>G	ENSP00000355746.2:p.Leu362Arg
ENST00000366783.8:c.1085T>G MANE Select	ENSP00000355747.3:p.Leu362Arg
ENST00000471728.2:n.1723T>G
ENST00000524196.6:c.1085T>G	ENSP00000429036.2:p.Leu362Arg
ENST00000626989.3:c.1085T>G	ENSP00000486498.2:p.Leu362Arg
ENST00000676467.1:c.*912T>G	ENSP00000504294.1:n.*912T>G
ENST00000676747.1:c.1082T>G	ENSP00000503244.1:p.Leu361Arg
ENST00000676884.1:c.1085T>G	ENSP00000503200.1:p.Leu362Arg
ENST00000676888.1:c.*426T>G	ENSP00000504483.1:n.*426T>G
ENST00000676907.1:c.*664T>G	ENSP00000504410.1:n.*664T>G
ENST00000676945.1:c.1085T>G	ENSP00000504433.1:p.Leu362Arg
ENST00000677065.1:n.1646T>G
ENST00000677414.1:c.1085T>G	ENSP00000503116.1:p.Leu362Arg
ENST00000677529.1:n.2815T>G
ENST00000677596.1:c.*1307T>G	ENSP00000503618.1:n.*1307T>G
ENST00000677599.1:c.1085T>G	ENSP00000503673.1:p.Leu362Arg
ENST00000677748.1:n.3340T>G
ENST00000677880.1:c.650T>G	ENSP00000503121.1:p.Leu217Arg
ENST00000678021.1:c.*708T>G	ENSP00000504674.1:n.*708T>G
ENST00000678233.1:c.1085T>G	ENSP00000504728.1:p.Leu362Arg
ENST00000678320.1:c.986T>G	ENSP00000503680.1:p.Leu329Arg
ENST00000678655.1:c.986T>G	ENSP00000504230.1:p.Leu329Arg
ENST00000678706.1:c.*462T>G	ENSP00000503659.1:n.*462T>G
ENST00000678776.1:c.*1222T>G	ENSP00000504624.1:n.*1222T>G
ENST00000678784.1:c.1072+2175T>G	ENSP00000504652.1:n.1072+2175T>G
ENST00000678820.1:c.983T>G	ENSP00000504138.1:p.Leu328Arg
ENST00000678835.1:c.*756+2175T>G	ENSP00000504343.1:n.*756+2175T>G
ENST00000679088.1:c.1085T>G	ENSP00000504727.1:p.Leu362Arg
ENST00000679098.1:c.1085T>G	ENSP00000504303.1:p.Leu362Arg
ENST00000366782.5:c.1184T>G	ENSP00000355746.1:p.Leu395Arg
ENST00000366783.7:c.1085T>G	ENSP00000355747.3:p.Leu362Arg
ENST00000422240.6:c.1082T>G	ENSP00000403737.2:p.Leu361Arg
ENST00000471728.1:n.343T>G
ENST00000472139.2:c.653T>G	ENSP00000427806.1:p.Leu218Arg
ENST00000626989.2:c.1184T>G	ENSP00000486498.1:p.Leu395Arg
NM_000447.2:c.1085T>G	NP_000438.2:p.Leu362Arg
NM_012486.2:c.1082T>G	NP_036618.2:p.Leu361Arg
XM_005273199.2:c.1085T>G	XP_005273256.1:p.Leu362Arg
XM_011544236.1:c.653T>G	XP_011542538.1:p.Leu218Arg
XR_949149.1:n.1819T>G
XM_005273199.4:c.1085T>G	XP_005273256.1:p.Leu362Arg
XM_017001835.1:c.1085T>G	XP_016857324.1:p.Leu362Arg
XM_017001836.1:c.1082T>G	XP_016857325.1:p.Leu361Arg
XR_001737316.2:n.1477+2175T>G
XR_001737317.2:n.1477+2175T>G
XR_001737318.2:n.1800T>G
XR_001737319.1:n.2143T>G
XR_001737320.1:n.2140T>G
XR_001737321.1:n.1635T>G
XR_949149.2:n.1797T>G
XR_949150.3:n.2016T>G
NM_000447.3:c.1085T>G MANE Select	NP_000438.2:p.Leu362Arg
NM_012486.3:c.1082T>G	NP_036618.2:p.Leu361Arg