Canonical Allele Identifier: CA1143441804
Gene: PSEN2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226895544A= , CM000663.2:g.226895544A= GRCh38
NC_000001.10:g.227083245A= , CM000663.1:g.227083245A= GRCh37
NC_000001.9:g.225149868A= NCBI36
NG_007381.1:g.29973A=
NG_012825.2:g.3009A=
NG_007381.2:g.30361A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.1312A= ENSP00000355741.2:p.Met438=
ENST00000366782.6:c.1312A= ENSP00000355746.2:p.Met438=
ENST00000366783.8:c.1312A= MANE Select ENSP00000355747.3:p.Met438=
ENST00000471728.2:n.1950A=
ENST00000524196.6:c.1312A= ENSP00000429036.2:p.Met438=
ENST00000626989.3:c.1312A= ENSP00000486498.2:p.Met438=
ENST00000676467.1:c.*1139A= ENSP00000504294.1:n.*1139A=
ENST00000676747.1:c.1188+1419A= ENSP00000503244.1:n.1188+1419A=
ENST00000676884.1:c.1312A= ENSP00000503200.1:p.Met438=
ENST00000676888.1:c.*653A= ENSP00000504483.1:n.*653A=
ENST00000676907.1:c.*891A= ENSP00000504410.1:n.*891A=
ENST00000676945.1:c.1191+1419A= ENSP00000504433.1:n.1191+1419A=
ENST00000677065.1:n.1873A=
ENST00000677414.1:c.1312A= ENSP00000503116.1:p.Met438=
ENST00000677529.1:n.3042A=
ENST00000677596.1:c.*1534A= ENSP00000503618.1:n.*1534A=
ENST00000677599.1:c.1191+1419A= ENSP00000503673.1:n.1191+1419A=
ENST00000677748.1:n.3567A=
ENST00000677880.1:c.877A= ENSP00000503121.1:p.Met293=
ENST00000678021.1:c.*935A= ENSP00000504674.1:n.*935A=
ENST00000678233.1:c.1312A= ENSP00000504728.1:p.Met438=
ENST00000678320.1:c.1213A= ENSP00000503680.1:p.Met405=
ENST00000678655.1:c.1092+1419A= ENSP00000504230.1:n.1092+1419A=
ENST00000678706.1:c.*689A= ENSP00000503659.1:n.*689A=
ENST00000678776.1:c.*1449A= ENSP00000504624.1:n.*1449A=
ENST00000678784.1:c.1073-2176A= ENSP00000504652.1:n.1073-2176A=
ENST00000678820.1:c.1089+1419A= ENSP00000504138.1:n.1089+1419A=
ENST00000678835.1:c.*757-2176A= ENSP00000504343.1:n.*757-2176A=
ENST00000679088.1:c.1312A= ENSP00000504727.1:p.Met438=
ENST00000679098.1:c.1312A= ENSP00000504303.1:p.Met438=
ENST00000366782.5:c.1411A= ENSP00000355746.1:p.Met471=
ENST00000366783.7:c.1312A= ENSP00000355747.3:p.Met438=
ENST00000422240.6:c.1309A= ENSP00000403737.2:p.Met437=
ENST00000471728.1:n.570A=
ENST00000472139.2:c.880A= ENSP00000427806.1:p.Met294=
ENST00000626989.2:c.1411A= ENSP00000486498.1:p.Met471=
NM_000447.2:c.1312A= NP_000438.2:p.Met438=
NM_012486.2:c.1309A= NP_036618.2:p.Met437=
XM_005273199.2:c.1312A= XP_005273256.1:p.Met438=
XM_011544236.1:c.880A= XP_011542538.1:p.Met294=
XR_949149.1:n.2046A=
XM_005273199.4:c.1312A= XP_005273256.1:p.Met438=
XM_017001835.1:c.1312A= XP_016857324.1:p.Met438=
XM_017001836.1:c.1309A= XP_016857325.1:p.Met437=
XR_001737316.2:n.1478-2176A=
XR_001737317.2:n.1478-2176A=
XR_001737318.2:n.2027A=
XR_001737319.1:n.2370A=
XR_001737320.1:n.2367A=
XR_001737321.1:n.1862A=
XR_949149.2:n.2024A=
XR_949150.3:n.2243A=
NM_000447.3:c.1312A= MANE Select NP_000438.2:p.Met438=
NM_012486.3:c.1309A= NP_036618.2:p.Met437=