Canonical Allele Identifier: CA2650783838

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226870636-CGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226870637_226870638del , CM000663.2:g.226870637_226870638del	GRCh38
NC_000001.10:g.227058338_227058339del , CM000663.1:g.227058338_227058339del	GRCh37
NC_000001.9:g.225124961_225124962del	NCBI36
NG_007381.1:g.5066_5067del
NG_007381.2:g.5454_5455del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.-350+132_-350+133del	ENSP00000355741.2:n.-350+132_-350+133del
ENST00000366783.8:c.-362_-361del MANE Select	ENSP00000355747.3:n.-362_-361del
ENST00000524196.6:c.-350+132_-350+133del	ENSP00000429036.2:n.-350+132_-350+133del
ENST00000676747.1:c.-219_-218del	ENSP00000503244.1:n.-219_-218del
ENST00000676840.1:c.-362_-361del	ENSP00000504318.1:n.-362_-361del
ENST00000676884.1:c.-350+132_-350+133del	ENSP00000503200.1:n.-350+132_-350+133del
ENST00000676888.1:c.-350+132_-350+133del	ENSP00000504483.1:n.-350+132_-350+133del
ENST00000676907.1:c.-362_-361del	ENSP00000504410.1:n.-362_-361del
ENST00000676945.1:c.-362_-361del	ENSP00000504433.1:n.-362_-361del
ENST00000677414.1:c.-219_-218del	ENSP00000503116.1:n.-219_-218del
ENST00000677529.1:n.77_78del
ENST00000677596.1:c.-362_-361del	ENSP00000503618.1:n.-362_-361del
ENST00000677599.1:c.-362_-361del	ENSP00000503673.1:n.-362_-361del
ENST00000677748.1:n.77_78del
ENST00000677880.1:c.-495_-494del	ENSP00000503121.1:n.-495_-494del
ENST00000678021.1:c.-362_-361del	ENSP00000504674.1:n.-362_-361del
ENST00000678233.1:c.-362_-361del	ENSP00000504728.1:n.-362_-361del
ENST00000678320.1:c.-362_-361del	ENSP00000503680.1:n.-362_-361del
ENST00000678655.1:c.-362_-361del	ENSP00000504230.1:n.-362_-361del
ENST00000678706.1:c.-362_-361del	ENSP00000503659.1:n.-362_-361del
ENST00000678784.1:c.-362_-361del	ENSP00000504652.1:n.-362_-361del
ENST00000678820.1:c.-362_-361del	ENSP00000504138.1:n.-362_-361del
ENST00000678835.1:c.-362_-361del	ENSP00000504343.1:n.-362_-361del
ENST00000679088.1:c.-1810_-1809del	ENSP00000504727.1:n.-1810_-1809del
ENST00000679098.1:c.-362_-361del	ENSP00000504303.1:n.-362_-361del
ENST00000366783.7:c.-362_-361del	ENSP00000355747.3:n.-362_-361del
ENST00000422240.6:c.-362_-361del	ENSP00000403737.2:n.-362_-361del
ENST00000495488.5:c.-219_-218del	ENSP00000429682.1:n.-219_-218del
ENST00000524196.5:c.-350+132_-350+133del	ENSP00000429036.1:n.-350+132_-350+133del
NM_000447.2:c.-362_-361del	NP_000438.2:n.-362_-361del
NM_012486.2:c.-362_-361del	NP_036618.2:n.-362_-361del
XM_005273199.2:c.-219_-218del	XP_005273256.1:n.-219_-218del
XR_949149.1:n.66_67del
XR_949150.1:n.66_67del
XM_005273199.4:c.-219_-218del	XP_005273256.1:n.-219_-218del
XM_017001836.1:c.-219_-218del	XP_016857325.1:n.-219_-218del
XR_001737316.2:n.44_45del
XR_001737317.2:n.44_45del
XR_001737318.2:n.44_45del
XR_001737321.1:n.22_23del
XR_949149.2:n.44_45del
XR_949150.3:n.44_45del
NM_000447.3:c.-362_-361del MANE Select	NP_000438.2:n.-362_-361del
NM_012486.3:c.-362_-361del	NP_036618.2:n.-362_-361del