Canonical Allele Identifier: CA1225084662

Gene: PSEN2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894123A= , CM000663.2:g.226894123A=	GRCh38
NC_000001.10:g.227081824A= , CM000663.1:g.227081824A=	GRCh37
NC_000001.9:g.225148447A=	NCBI36
NG_007381.1:g.28552A=
NG_012825.2:g.1588A=
NG_007381.2:g.28940A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1189A=	ENSP00000355741.2:p.Ile397=
ENST00000366782.6:c.1189A=	ENSP00000355746.2:p.Ile397=
ENST00000366783.8:c.1189A= MANE Select	ENSP00000355747.3:p.Ile397=
ENST00000471728.2:n.1827A=
ENST00000524196.6:c.1189A=	ENSP00000429036.2:p.Ile397=
ENST00000626989.3:c.1189A=	ENSP00000486498.2:p.Ile397=
ENST00000676467.1:c.*1016A=	ENSP00000504294.1:n.*1016A=
ENST00000676747.1:c.1186A=	ENSP00000503244.1:p.Ile396=
ENST00000676884.1:c.1189A=	ENSP00000503200.1:p.Ile397=
ENST00000676888.1:c.*530A=	ENSP00000504483.1:n.*530A=
ENST00000676907.1:c.*768A=	ENSP00000504410.1:n.*768A=
ENST00000676945.1:c.1189A=	ENSP00000504433.1:p.Ile397=
ENST00000677065.1:n.1750A=
ENST00000677414.1:c.1189A=	ENSP00000503116.1:p.Ile397=
ENST00000677529.1:n.2919A=
ENST00000677596.1:c.*1411A=	ENSP00000503618.1:n.*1411A=
ENST00000677599.1:c.1189A=	ENSP00000503673.1:p.Ile397=
ENST00000677748.1:n.3444A=
ENST00000677880.1:c.754A=	ENSP00000503121.1:p.Ile252=
ENST00000678021.1:c.*812A=	ENSP00000504674.1:n.*812A=
ENST00000678233.1:c.1189A=	ENSP00000504728.1:p.Ile397=
ENST00000678320.1:c.1090A=	ENSP00000503680.1:p.Ile364=
ENST00000678655.1:c.1090A=	ENSP00000504230.1:p.Ile364=
ENST00000678706.1:c.*566A=	ENSP00000503659.1:n.*566A=
ENST00000678776.1:c.*1326A=	ENSP00000504624.1:n.*1326A=
ENST00000678784.1:c.1072+2279A=	ENSP00000504652.1:n.1072+2279A=
ENST00000678820.1:c.1087A=	ENSP00000504138.1:p.Ile363=
ENST00000678835.1:c.*756+2279A=	ENSP00000504343.1:n.*756+2279A=
ENST00000679088.1:c.1189A=	ENSP00000504727.1:p.Ile397=
ENST00000679098.1:c.1189A=	ENSP00000504303.1:p.Ile397=
ENST00000366782.5:c.1288A=	ENSP00000355746.1:p.Ile430=
ENST00000366783.7:c.1189A=	ENSP00000355747.3:p.Ile397=
ENST00000422240.6:c.1186A=	ENSP00000403737.2:p.Ile396=
ENST00000471728.1:n.447A=
ENST00000472139.2:c.757A=	ENSP00000427806.1:p.Ile253=
ENST00000626989.2:c.1288A=	ENSP00000486498.1:p.Ile430=
NM_000447.2:c.1189A=	NP_000438.2:p.Ile397=
NM_012486.2:c.1186A=	NP_036618.2:p.Ile396=
XM_005273199.2:c.1189A=	XP_005273256.1:p.Ile397=
XM_011544236.1:c.757A=	XP_011542538.1:p.Ile253=
XR_949149.1:n.1923A=
XM_005273199.4:c.1189A=	XP_005273256.1:p.Ile397=
XM_017001835.1:c.1189A=	XP_016857324.1:p.Ile397=
XM_017001836.1:c.1186A=	XP_016857325.1:p.Ile396=
XR_001737316.2:n.1477+2279A=
XR_001737317.2:n.1477+2279A=
XR_001737318.2:n.1904A=
XR_001737319.1:n.2247A=
XR_001737320.1:n.2244A=
XR_001737321.1:n.1739A=
XR_949149.2:n.1901A=
XR_949150.3:n.2120A=
NM_000447.3:c.1189A= MANE Select	NP_000438.2:p.Ile397=
NM_012486.3:c.1186A=	NP_036618.2:p.Ile396=