Canonical Allele Identifier: CA2650788620

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226896088-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226896088T>C , CM000663.2:g.226896088T>C	GRCh38
NC_000001.10:g.227083789T>C , CM000663.1:g.227083789T>C	GRCh37
NC_000001.9:g.225150412T>C	NCBI36
NG_007381.1:g.30517T>C
NG_012825.2:g.3553T>C
NG_007381.2:g.30905T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*509T>C	ENSP00000355741.2:n.*509T>C
ENST00000366782.6:c.*509T>C	ENSP00000355746.2:n.*509T>C
ENST00000366783.8:c.*509T>C MANE Select	ENSP00000355747.3:n.*509T>C
ENST00000524196.6:c.*509T>C	ENSP00000429036.2:n.*509T>C
ENST00000626989.3:c.*509T>C	ENSP00000486498.2:n.*509T>C
ENST00000676747.1:c.1189-1632T>C	ENSP00000503244.1:n.1189-1632T>C
ENST00000676884.1:c.*509T>C	ENSP00000503200.1:n.*509T>C
ENST00000676945.1:c.1191+1963T>C	ENSP00000504433.1:n.1191+1963T>C
ENST00000677414.1:c.*509T>C	ENSP00000503116.1:n.*509T>C
ENST00000677599.1:c.1191+1963T>C	ENSP00000503673.1:n.1191+1963T>C
ENST00000678233.1:c.*8+501T>C	ENSP00000504728.1:n.*8+501T>C
ENST00000678655.1:c.1093-1632T>C	ENSP00000504230.1:n.1093-1632T>C
ENST00000678784.1:c.1073-1632T>C	ENSP00000504652.1:n.1073-1632T>C
ENST00000678820.1:c.1090-1632T>C	ENSP00000504138.1:n.1090-1632T>C
ENST00000678835.1:c.*757-1632T>C	ENSP00000504343.1:n.*757-1632T>C
ENST00000679088.1:c.*509T>C	ENSP00000504727.1:n.*509T>C
ENST00000679098.1:c.*8+501T>C	ENSP00000504303.1:n.*8+501T>C
ENST00000366782.5:c.*509T>C	ENSP00000355746.1:n.*509T>C
ENST00000366783.7:c.*509T>C	ENSP00000355747.3:n.*509T>C
ENST00000626989.2:c.1955T>C	ENSP00000486498.1:n.1955T>C
NM_000447.2:c.*509T>C	NP_000438.2:n.*509T>C
NM_012486.2:c.*509T>C	NP_036618.2:n.*509T>C
XM_005273199.2:c.*509T>C	XP_005273256.1:n.*509T>C
XM_011544236.1:c.*509T>C	XP_011542538.1:n.*509T>C
XM_005273199.4:c.*509T>C	XP_005273256.1:n.*509T>C
XM_017001835.1:c.*509T>C	XP_016857324.1:n.*509T>C
XM_017001836.1:c.*509T>C	XP_016857325.1:n.*509T>C
XR_001737316.2:n.1478-1632T>C
XR_001737317.2:n.1478-1632T>C
XR_001737318.2:n.2571T>C
XR_001737319.1:n.2914T>C
XR_001737320.1:n.2911T>C
XR_001737321.1:n.2406T>C
XR_949149.2:n.2568T>C
XR_949150.3:n.2787T>C
NM_000447.3:c.*509T>C MANE Select	NP_000438.2:n.*509T>C
NM_012486.3:c.*509T>C	NP_036618.2:n.*509T>C