Canonical Allele Identifier: CA1225072677
Gene: PSEN2 HGNC NCBI

Linked Data

dbSNP Id: rs1660199445

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.226870592_226870597del , CM000663.2:g.226870592_226870597del GRCh38
NC_000001.10:g.227058293_227058298del , CM000663.1:g.227058293_227058298del GRCh37
NC_000001.9:g.225124916_225124921del NCBI36
NG_007381.1:g.5021_5026del
NG_007381.2:g.5409_5414del

Transcript Alleles

HGVS Amino-acid Change
ENST00000366779.6:c.-350+87_-350+92del ENSP00000355741.2:n.-350+87_-350+92del
ENST00000524196.6:c.-350+87_-350+92del ENSP00000429036.2:n.-350+87_-350+92del
ENST00000676840.1:c.-407_-402del ENSP00000504318.1:n.-407_-402del
ENST00000676884.1:c.-350+87_-350+92del ENSP00000503200.1:n.-350+87_-350+92del
ENST00000676888.1:c.-350+87_-350+92del ENSP00000504483.1:n.-350+87_-350+92del
ENST00000676907.1:c.-407_-402del ENSP00000504410.1:n.-407_-402del
ENST00000676945.1:c.-407_-402del ENSP00000504433.1:n.-407_-402del
ENST00000677414.1:c.-264_-259del ENSP00000503116.1:n.-264_-259del
ENST00000677529.1:n.32_37del
ENST00000677599.1:c.-407_-402del ENSP00000503673.1:n.-407_-402del
ENST00000677748.1:n.32_37del
ENST00000678233.1:c.-407_-402del ENSP00000504728.1:n.-407_-402del
ENST00000678320.1:c.-407_-402del ENSP00000503680.1:n.-407_-402del
ENST00000678655.1:c.-407_-402del ENSP00000504230.1:n.-407_-402del
ENST00000678706.1:c.-407_-402del ENSP00000503659.1:n.-407_-402del
ENST00000678784.1:c.-407_-402del ENSP00000504652.1:n.-407_-402del
ENST00000678820.1:c.-407_-402del ENSP00000504138.1:n.-407_-402del
ENST00000678835.1:c.-407_-402del ENSP00000504343.1:n.-407_-402del
ENST00000679098.1:c.-407_-402del ENSP00000504303.1:n.-407_-402del
ENST00000366783.7:c.-407_-402del ENSP00000355747.3:n.-407_-402del
ENST00000524196.5:c.-350+87_-350+92del ENSP00000429036.1:n.-350+87_-350+92del
NM_000447.2:c.-407_-402del NP_000438.2:n.-407_-402del
NM_012486.2:c.-407_-402del NP_036618.2:n.-407_-402del
XR_949149.1:n.21_26del
XR_949150.1:n.21_26del