Canonical Allele Identifier: CA423519751

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227081772C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894071C>G , CM000663.2:g.226894071C>G	GRCh38
NC_000001.10:g.227081772C>G , CM000663.1:g.227081772C>G	GRCh37
NC_000001.9:g.225148395C>G	NCBI36
NG_007381.1:g.28500C>G
NG_012825.2:g.1536C>G
NG_007381.2:g.28888C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1137C>G	ENSP00000355741.2:p.Ala379=
ENST00000366782.6:c.1137C>G	ENSP00000355746.2:p.Ala379=
ENST00000366783.8:c.1137C>G MANE Select	ENSP00000355747.3:p.Ala379=
ENST00000471728.2:n.1775C>G
ENST00000524196.6:c.1137C>G	ENSP00000429036.2:p.Ala379=
ENST00000626989.3:c.1137C>G	ENSP00000486498.2:p.Ala379=
ENST00000676467.1:c.*964C>G	ENSP00000504294.1:n.*964C>G
ENST00000676747.1:c.1134C>G	ENSP00000503244.1:p.Ala378=
ENST00000676884.1:c.1137C>G	ENSP00000503200.1:p.Ala379=
ENST00000676888.1:c.*478C>G	ENSP00000504483.1:n.*478C>G
ENST00000676907.1:c.*716C>G	ENSP00000504410.1:n.*716C>G
ENST00000676945.1:c.1137C>G	ENSP00000504433.1:p.Ala379=
ENST00000677065.1:n.1698C>G
ENST00000677414.1:c.1137C>G	ENSP00000503116.1:p.Ala379=
ENST00000677529.1:n.2867C>G
ENST00000677596.1:c.*1359C>G	ENSP00000503618.1:n.*1359C>G
ENST00000677599.1:c.1137C>G	ENSP00000503673.1:p.Ala379=
ENST00000677748.1:n.3392C>G
ENST00000677880.1:c.702C>G	ENSP00000503121.1:p.Ala234=
ENST00000678021.1:c.*760C>G	ENSP00000504674.1:n.*760C>G
ENST00000678233.1:c.1137C>G	ENSP00000504728.1:p.Ala379=
ENST00000678320.1:c.1038C>G	ENSP00000503680.1:p.Ala346=
ENST00000678655.1:c.1038C>G	ENSP00000504230.1:p.Ala346=
ENST00000678706.1:c.*514C>G	ENSP00000503659.1:n.*514C>G
ENST00000678776.1:c.*1274C>G	ENSP00000504624.1:n.*1274C>G
ENST00000678784.1:c.1072+2227C>G	ENSP00000504652.1:n.1072+2227C>G
ENST00000678820.1:c.1035C>G	ENSP00000504138.1:p.Ala345=
ENST00000678835.1:c.*756+2227C>G	ENSP00000504343.1:n.*756+2227C>G
ENST00000679088.1:c.1137C>G	ENSP00000504727.1:p.Ala379=
ENST00000679098.1:c.1137C>G	ENSP00000504303.1:p.Ala379=
ENST00000366782.5:c.1236C>G	ENSP00000355746.1:p.Ala412=
ENST00000366783.7:c.1137C>G	ENSP00000355747.3:p.Ala379=
ENST00000422240.6:c.1134C>G	ENSP00000403737.2:p.Ala378=
ENST00000471728.1:n.395C>G
ENST00000472139.2:c.705C>G	ENSP00000427806.1:p.Ala235=
ENST00000626989.2:c.1236C>G	ENSP00000486498.1:p.Ala412=
NM_000447.2:c.1137C>G	NP_000438.2:p.Ala379=
NM_012486.2:c.1134C>G	NP_036618.2:p.Ala378=
XM_005273199.2:c.1137C>G	XP_005273256.1:p.Ala379=
XM_011544236.1:c.705C>G	XP_011542538.1:p.Ala235=
XR_949149.1:n.1871C>G
XM_005273199.4:c.1137C>G	XP_005273256.1:p.Ala379=
XM_017001835.1:c.1137C>G	XP_016857324.1:p.Ala379=
XM_017001836.1:c.1134C>G	XP_016857325.1:p.Ala378=
XR_001737316.2:n.1477+2227C>G
XR_001737317.2:n.1477+2227C>G
XR_001737318.2:n.1852C>G
XR_001737319.1:n.2195C>G
XR_001737320.1:n.2192C>G
XR_001737321.1:n.1687C>G
XR_949149.2:n.1849C>G
XR_949150.3:n.2068C>G
NM_000447.3:c.1137C>G MANE Select	NP_000438.2:p.Ala379=
NM_012486.3:c.1134C>G	NP_036618.2:p.Ala378=