Canonical Allele Identifier: CA423520695

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083187C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895486C>A , CM000663.2:g.226895486C>A	GRCh38
NC_000001.10:g.227083187C>A , CM000663.1:g.227083187C>A	GRCh37
NC_000001.9:g.225149810C>A	NCBI36
NG_007381.1:g.29915C>A
NG_012825.2:g.2951C>A
NG_007381.2:g.30303C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1254C>A	ENSP00000355741.2:p.Ile418=
ENST00000366782.6:c.1254C>A	ENSP00000355746.2:p.Ile418=
ENST00000366783.8:c.1254C>A MANE Select	ENSP00000355747.3:p.Ile418=
ENST00000471728.2:n.1892C>A
ENST00000524196.6:c.1254C>A	ENSP00000429036.2:p.Ile418=
ENST00000626989.3:c.1254C>A	ENSP00000486498.2:p.Ile418=
ENST00000676467.1:c.*1081C>A	ENSP00000504294.1:n.*1081C>A
ENST00000676747.1:c.1188+1361C>A	ENSP00000503244.1:n.1188+1361C>A
ENST00000676884.1:c.1254C>A	ENSP00000503200.1:p.Ile418=
ENST00000676888.1:c.*595C>A	ENSP00000504483.1:n.*595C>A
ENST00000676907.1:c.*833C>A	ENSP00000504410.1:n.*833C>A
ENST00000676945.1:c.1191+1361C>A	ENSP00000504433.1:n.1191+1361C>A
ENST00000677065.1:n.1815C>A
ENST00000677414.1:c.1254C>A	ENSP00000503116.1:p.Ile418=
ENST00000677529.1:n.2984C>A
ENST00000677596.1:c.*1476C>A	ENSP00000503618.1:n.*1476C>A
ENST00000677599.1:c.1191+1361C>A	ENSP00000503673.1:n.1191+1361C>A
ENST00000677748.1:n.3509C>A
ENST00000677880.1:c.819C>A	ENSP00000503121.1:p.Ile273=
ENST00000678021.1:c.*877C>A	ENSP00000504674.1:n.*877C>A
ENST00000678233.1:c.1254C>A	ENSP00000504728.1:p.Ile418=
ENST00000678320.1:c.1155C>A	ENSP00000503680.1:p.Ile385=
ENST00000678655.1:c.1092+1361C>A	ENSP00000504230.1:n.1092+1361C>A
ENST00000678706.1:c.*631C>A	ENSP00000503659.1:n.*631C>A
ENST00000678776.1:c.*1391C>A	ENSP00000504624.1:n.*1391C>A
ENST00000678784.1:c.1073-2234C>A	ENSP00000504652.1:n.1073-2234C>A
ENST00000678820.1:c.1089+1361C>A	ENSP00000504138.1:n.1089+1361C>A
ENST00000678835.1:c.*757-2234C>A	ENSP00000504343.1:n.*757-2234C>A
ENST00000679088.1:c.1254C>A	ENSP00000504727.1:p.Ile418=
ENST00000679098.1:c.1254C>A	ENSP00000504303.1:p.Ile418=
ENST00000366782.5:c.1353C>A	ENSP00000355746.1:p.Ile451=
ENST00000366783.7:c.1254C>A	ENSP00000355747.3:p.Ile418=
ENST00000422240.6:c.1251C>A	ENSP00000403737.2:p.Ile417=
ENST00000471728.1:n.512C>A
ENST00000472139.2:c.822C>A	ENSP00000427806.1:p.Ile274=
ENST00000626989.2:c.1353C>A	ENSP00000486498.1:p.Ile451=
NM_000447.2:c.1254C>A	NP_000438.2:p.Ile418=
NM_012486.2:c.1251C>A	NP_036618.2:p.Ile417=
XM_005273199.2:c.1254C>A	XP_005273256.1:p.Ile418=
XM_011544236.1:c.822C>A	XP_011542538.1:p.Ile274=
XR_949149.1:n.1988C>A
XM_005273199.4:c.1254C>A	XP_005273256.1:p.Ile418=
XM_017001835.1:c.1254C>A	XP_016857324.1:p.Ile418=
XM_017001836.1:c.1251C>A	XP_016857325.1:p.Ile417=
XR_001737316.2:n.1478-2234C>A
XR_001737317.2:n.1478-2234C>A
XR_001737318.2:n.1969C>A
XR_001737319.1:n.2312C>A
XR_001737320.1:n.2309C>A
XR_001737321.1:n.1804C>A
XR_949149.2:n.1966C>A
XR_949150.3:n.2185C>A
NM_000447.3:c.1254C>A MANE Select	NP_000438.2:p.Ile418=
NM_012486.3:c.1251C>A	NP_036618.2:p.Ile417=