Canonical Allele Identifier: CA2650788614

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226896075-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226896076del , CM000663.2:g.226896076del	GRCh38
NC_000001.10:g.227083777del , CM000663.1:g.227083777del	GRCh37
NC_000001.9:g.225150400del	NCBI36
NG_007381.1:g.30505del
NG_012825.2:g.3541del
NG_007381.2:g.30893del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*497del	ENSP00000355741.2:n.*497del
ENST00000366782.6:c.*497del	ENSP00000355746.2:n.*497del
ENST00000366783.8:c.*497del MANE Select	ENSP00000355747.3:n.*497del
ENST00000471728.2:n.2482del
ENST00000524196.6:c.*497del	ENSP00000429036.2:n.*497del
ENST00000626989.3:c.*497del	ENSP00000486498.2:n.*497del
ENST00000676467.1:c.*1671del	ENSP00000504294.1:n.*1671del
ENST00000676747.1:c.1189-1644del	ENSP00000503244.1:n.1189-1644del
ENST00000676884.1:c.*497del	ENSP00000503200.1:n.*497del
ENST00000676888.1:c.*1185del	ENSP00000504483.1:n.*1185del
ENST00000676907.1:c.*1423del	ENSP00000504410.1:n.*1423del
ENST00000676945.1:c.1191+1951del	ENSP00000504433.1:n.1191+1951del
ENST00000677065.1:n.2405del
ENST00000677414.1:c.*497del	ENSP00000503116.1:n.*497del
ENST00000677529.1:n.3574del
ENST00000677596.1:c.*2066del	ENSP00000503618.1:n.*2066del
ENST00000677599.1:c.1191+1951del	ENSP00000503673.1:n.1191+1951del
ENST00000677748.1:n.4099del
ENST00000677880.1:c.*497del	ENSP00000503121.1:n.*497del
ENST00000678021.1:c.*1467del	ENSP00000504674.1:n.*1467del
ENST00000678233.1:c.*8+489del	ENSP00000504728.1:n.*8+489del
ENST00000678320.1:c.*497del	ENSP00000503680.1:n.*497del
ENST00000678655.1:c.1093-1644del	ENSP00000504230.1:n.1093-1644del
ENST00000678706.1:c.*1221del	ENSP00000503659.1:n.*1221del
ENST00000678776.1:c.*1981del	ENSP00000504624.1:n.*1981del
ENST00000678784.1:c.1073-1644del	ENSP00000504652.1:n.1073-1644del
ENST00000678820.1:c.1090-1644del	ENSP00000504138.1:n.1090-1644del
ENST00000678835.1:c.*757-1644del	ENSP00000504343.1:n.*757-1644del
ENST00000679088.1:c.*497del	ENSP00000504727.1:n.*497del
ENST00000679098.1:c.*8+489del	ENSP00000504303.1:n.*8+489del
ENST00000366782.5:c.*497del	ENSP00000355746.1:n.*497del
ENST00000366783.7:c.*497del	ENSP00000355747.3:n.*497del
ENST00000626989.2:c.1943del	ENSP00000486498.1:n.1943del
NM_000447.2:c.*497del	NP_000438.2:n.*497del
NM_012486.2:c.*497del	NP_036618.2:n.*497del
XM_005273199.2:c.*497del	XP_005273256.1:n.*497del
XM_011544236.1:c.*497del	XP_011542538.1:n.*497del
XM_005273199.4:c.*497del	XP_005273256.1:n.*497del
XM_017001835.1:c.*497del	XP_016857324.1:n.*497del
XM_017001836.1:c.*497del	XP_016857325.1:n.*497del
XR_001737316.2:n.1478-1644del
XR_001737317.2:n.1478-1644del
XR_001737318.2:n.2559del
XR_001737319.1:n.2902del
XR_001737320.1:n.2899del
XR_001737321.1:n.2394del
XR_949149.2:n.2556del
XR_949150.3:n.2775del
NM_000447.3:c.*497del MANE Select	NP_000438.2:n.*497del
NM_012486.3:c.*497del	NP_036618.2:n.*497del