Canonical Allele Identifier: CA38616585
Gene: PSEN2 HGNC NCBI

Linked Data

dbSNP Id: rs199654606

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226885636T>C , CM000663.2:g.226885636T>C GRCh38
NC_000001.10:g.227073337T>C , CM000663.1:g.227073337T>C GRCh37
NC_000001.9:g.225139960T>C NCBI36
NG_007381.1:g.20065T>C
NG_007381.2:g.20453T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000366779.6:c.455T>C ENSP00000355741.2:p.Met152Thr
ENST00000366782.6:c.455T>C ENSP00000355746.2:p.Met152Thr
ENST00000366783.8:c.455T>C MANE Select ENSP00000355747.3:p.Met152Thr
ENST00000524196.6:c.455T>C ENSP00000429036.2:p.Met152Thr
ENST00000626989.3:c.455T>C ENSP00000486498.2:p.Met152Thr
ENST00000676467.1:c.*285T>C ENSP00000504294.1:p.=
ENST00000676747.1:c.455T>C ENSP00000503244.1:p.Met152Thr
ENST00000676840.1:c.455T>C ENSP00000504318.1:p.Met152Thr
ENST00000676884.1:c.455T>C ENSP00000503200.1:p.Met152Thr
ENST00000676888.1:c.455T>C ENSP00000504483.1:p.Met152Thr
ENST00000676907.1:c.*34T>C ENSP00000504410.1:p.=
ENST00000676945.1:c.455T>C ENSP00000504433.1:p.Met152Thr
ENST00000677065.1:n.1016T>C
ENST00000677414.1:c.455T>C ENSP00000503116.1:p.Met152Thr
ENST00000677529.1:n.893T>C
ENST00000677596.1:c.*362T>C ENSP00000503618.1:p.=
ENST00000677599.1:c.455T>C ENSP00000503673.1:p.Met152Thr
ENST00000677748.1:n.893T>C
ENST00000677880.1:c.23T>C ENSP00000503121.1:p.Met8Thr
ENST00000678021.1:c.*78T>C ENSP00000504674.1:p.=
ENST00000678233.1:c.455T>C ENSP00000504728.1:p.Met152Thr
ENST00000678320.1:c.455T>C ENSP00000503680.1:p.Met152Thr
ENST00000678655.1:c.455T>C ENSP00000504230.1:p.Met152Thr
ENST00000678706.1:c.455T>C ENSP00000503659.1:p.Met152Thr
ENST00000678776.1:c.*285T>C ENSP00000504624.1:p.=
ENST00000678784.1:c.455T>C ENSP00000504652.1:p.Met152Thr
ENST00000678820.1:c.455T>C ENSP00000504138.1:p.Met152Thr
ENST00000678835.1:c.455T>C ENSP00000504343.1:p.Met152Thr
ENST00000679088.1:c.455T>C ENSP00000504727.1:p.Met152Thr
ENST00000679098.1:c.455T>C ENSP00000504303.1:p.Met152Thr
ENST00000366782.5:c.554T>C ENSP00000355746.1:p.Met185Thr
ENST00000366783.7:c.455T>C ENSP00000355747.3:p.Met152Thr
ENST00000422240.6:c.455T>C ENSP00000403737.2:p.Met152Thr
ENST00000460775.5:c.-21-2455T>C ENSP00000427912.1:p.=
ENST00000472139.2:c.23T>C ENSP00000427806.1:p.Met8Thr
ENST00000626989.2:n.554T>C ENSP00000486498.1:p.Met185Thr
NM_000447.2:c.455T>C NP_000438.2:p.Met152Thr
NM_012486.2:c.455T>C NP_036618.2:p.Met152Thr
XM_005273199.2:c.455T>C XP_005273256.1:p.Met152Thr
XM_011544236.1:c.23T>C XP_011542538.1:p.Met8Thr
XR_949149.1:n.882T>C
XR_949150.1:n.882T>C
XM_005273199.4:c.455T>C XP_005273256.1:p.Met152Thr
XM_017001835.1:c.455T>C XP_016857324.1:p.Met152Thr
XM_017001836.1:c.455T>C XP_016857325.1:p.Met152Thr
XR_001737316.2:n.860T>C
XR_001737317.2:n.860T>C
XR_001737318.2:n.860T>C
XR_001737319.1:n.1203T>C
XR_001737320.1:n.1203T>C
XR_001737321.1:n.695T>C
XR_949149.2:n.860T>C
XR_949150.3:n.860T>C
NM_000447.3:c.455T>C MANE Select NP_000438.2:p.Met152Thr
NM_012486.3:c.455T>C NP_036618.2:p.Met152Thr