Canonical Allele Identifier: CA423520683

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226895483-C-T
• MyVariant Identifiers: chr1:g.227083184C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895483C>T , CM000663.2:g.226895483C>T	GRCh38
NC_000001.10:g.227083184C>T , CM000663.1:g.227083184C>T	GRCh37
NC_000001.9:g.225149807C>T	NCBI36
NG_007381.1:g.29912C>T
NG_012825.2:g.2948C>T
NG_007381.2:g.30300C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1251C>T	ENSP00000355741.2:p.Pro417=
ENST00000366782.6:c.1251C>T	ENSP00000355746.2:p.Pro417=
ENST00000366783.8:c.1251C>T MANE Select	ENSP00000355747.3:p.Pro417=
ENST00000471728.2:n.1889C>T
ENST00000524196.6:c.1251C>T	ENSP00000429036.2:p.Pro417=
ENST00000626989.3:c.1251C>T	ENSP00000486498.2:p.Pro417=
ENST00000676467.1:c.*1078C>T	ENSP00000504294.1:n.*1078C>T
ENST00000676747.1:c.1188+1358C>T	ENSP00000503244.1:n.1188+1358C>T
ENST00000676884.1:c.1251C>T	ENSP00000503200.1:p.Pro417=
ENST00000676888.1:c.*592C>T	ENSP00000504483.1:n.*592C>T
ENST00000676907.1:c.*830C>T	ENSP00000504410.1:n.*830C>T
ENST00000676945.1:c.1191+1358C>T	ENSP00000504433.1:n.1191+1358C>T
ENST00000677065.1:n.1812C>T
ENST00000677414.1:c.1251C>T	ENSP00000503116.1:p.Pro417=
ENST00000677529.1:n.2981C>T
ENST00000677596.1:c.*1473C>T	ENSP00000503618.1:n.*1473C>T
ENST00000677599.1:c.1191+1358C>T	ENSP00000503673.1:n.1191+1358C>T
ENST00000677748.1:n.3506C>T
ENST00000677880.1:c.816C>T	ENSP00000503121.1:p.Pro272=
ENST00000678021.1:c.*874C>T	ENSP00000504674.1:n.*874C>T
ENST00000678233.1:c.1251C>T	ENSP00000504728.1:p.Pro417=
ENST00000678320.1:c.1152C>T	ENSP00000503680.1:p.Pro384=
ENST00000678655.1:c.1092+1358C>T	ENSP00000504230.1:n.1092+1358C>T
ENST00000678706.1:c.*628C>T	ENSP00000503659.1:n.*628C>T
ENST00000678776.1:c.*1388C>T	ENSP00000504624.1:n.*1388C>T
ENST00000678784.1:c.1073-2237C>T	ENSP00000504652.1:n.1073-2237C>T
ENST00000678820.1:c.1089+1358C>T	ENSP00000504138.1:n.1089+1358C>T
ENST00000678835.1:c.*757-2237C>T	ENSP00000504343.1:n.*757-2237C>T
ENST00000679088.1:c.1251C>T	ENSP00000504727.1:p.Pro417=
ENST00000679098.1:c.1251C>T	ENSP00000504303.1:p.Pro417=
ENST00000366782.5:c.1350C>T	ENSP00000355746.1:p.Pro450=
ENST00000366783.7:c.1251C>T	ENSP00000355747.3:p.Pro417=
ENST00000422240.6:c.1248C>T	ENSP00000403737.2:p.Pro416=
ENST00000471728.1:n.509C>T
ENST00000472139.2:c.819C>T	ENSP00000427806.1:p.Pro273=
ENST00000626989.2:c.1350C>T	ENSP00000486498.1:p.Pro450=
NM_000447.2:c.1251C>T	NP_000438.2:p.Pro417=
NM_012486.2:c.1248C>T	NP_036618.2:p.Pro416=
XM_005273199.2:c.1251C>T	XP_005273256.1:p.Pro417=
XM_011544236.1:c.819C>T	XP_011542538.1:p.Pro273=
XR_949149.1:n.1985C>T
XM_005273199.4:c.1251C>T	XP_005273256.1:p.Pro417=
XM_017001835.1:c.1251C>T	XP_016857324.1:p.Pro417=
XM_017001836.1:c.1248C>T	XP_016857325.1:p.Pro416=
XR_001737316.2:n.1478-2237C>T
XR_001737317.2:n.1478-2237C>T
XR_001737318.2:n.1966C>T
XR_001737319.1:n.2309C>T
XR_001737320.1:n.2306C>T
XR_001737321.1:n.1801C>T
XR_949149.2:n.1963C>T
XR_949150.3:n.2182C>T
NM_000447.3:c.1251C>T MANE Select	NP_000438.2:p.Pro417=
NM_012486.3:c.1248C>T	NP_036618.2:p.Pro416=