Canonical Allele Identifier: CA2650788588

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226896025-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226896025T>C , CM000663.2:g.226896025T>C	GRCh38
NC_000001.10:g.227083726T>C , CM000663.1:g.227083726T>C	GRCh37
NC_000001.9:g.225150349T>C	NCBI36
NG_007381.1:g.30454T>C
NG_012825.2:g.3490T>C
NG_007381.2:g.30842T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.*446T>C	ENSP00000355741.2:n.*446T>C
ENST00000366782.6:c.*446T>C	ENSP00000355746.2:n.*446T>C
ENST00000366783.8:c.*446T>C MANE Select	ENSP00000355747.3:n.*446T>C
ENST00000471728.2:n.2431T>C
ENST00000524196.6:c.*446T>C	ENSP00000429036.2:n.*446T>C
ENST00000626989.3:c.*446T>C	ENSP00000486498.2:n.*446T>C
ENST00000676467.1:c.*1620T>C	ENSP00000504294.1:n.*1620T>C
ENST00000676747.1:c.1189-1695T>C	ENSP00000503244.1:n.1189-1695T>C
ENST00000676884.1:c.*446T>C	ENSP00000503200.1:n.*446T>C
ENST00000676888.1:c.*1134T>C	ENSP00000504483.1:n.*1134T>C
ENST00000676907.1:c.*1372T>C	ENSP00000504410.1:n.*1372T>C
ENST00000676945.1:c.1191+1900T>C	ENSP00000504433.1:n.1191+1900T>C
ENST00000677065.1:n.2354T>C
ENST00000677414.1:c.*446T>C	ENSP00000503116.1:n.*446T>C
ENST00000677529.1:n.3523T>C
ENST00000677596.1:c.*2015T>C	ENSP00000503618.1:n.*2015T>C
ENST00000677599.1:c.1191+1900T>C	ENSP00000503673.1:n.1191+1900T>C
ENST00000677748.1:n.4048T>C
ENST00000677880.1:c.*446T>C	ENSP00000503121.1:n.*446T>C
ENST00000678021.1:c.*1416T>C	ENSP00000504674.1:n.*1416T>C
ENST00000678233.1:c.*8+438T>C	ENSP00000504728.1:n.*8+438T>C
ENST00000678320.1:c.*446T>C	ENSP00000503680.1:n.*446T>C
ENST00000678655.1:c.1093-1695T>C	ENSP00000504230.1:n.1093-1695T>C
ENST00000678706.1:c.*1170T>C	ENSP00000503659.1:n.*1170T>C
ENST00000678776.1:c.*1930T>C	ENSP00000504624.1:n.*1930T>C
ENST00000678784.1:c.1073-1695T>C	ENSP00000504652.1:n.1073-1695T>C
ENST00000678820.1:c.1090-1695T>C	ENSP00000504138.1:n.1090-1695T>C
ENST00000678835.1:c.*757-1695T>C	ENSP00000504343.1:n.*757-1695T>C
ENST00000679088.1:c.*446T>C	ENSP00000504727.1:n.*446T>C
ENST00000679098.1:c.*8+438T>C	ENSP00000504303.1:n.*8+438T>C
ENST00000366782.5:c.*446T>C	ENSP00000355746.1:n.*446T>C
ENST00000366783.7:c.*446T>C	ENSP00000355747.3:n.*446T>C
ENST00000626989.2:c.1892T>C	ENSP00000486498.1:n.1892T>C
NM_000447.2:c.*446T>C	NP_000438.2:n.*446T>C
NM_012486.2:c.*446T>C	NP_036618.2:n.*446T>C
XM_005273199.2:c.*446T>C	XP_005273256.1:n.*446T>C
XM_011544236.1:c.*446T>C	XP_011542538.1:n.*446T>C
XM_005273199.4:c.*446T>C	XP_005273256.1:n.*446T>C
XM_017001835.1:c.*446T>C	XP_016857324.1:n.*446T>C
XM_017001836.1:c.*446T>C	XP_016857325.1:n.*446T>C
XR_001737316.2:n.1478-1695T>C
XR_001737317.2:n.1478-1695T>C
XR_001737318.2:n.2508T>C
XR_001737319.1:n.2851T>C
XR_001737320.1:n.2848T>C
XR_001737321.1:n.2343T>C
XR_949149.2:n.2505T>C
XR_949150.3:n.2724T>C
NM_000447.3:c.*446T>C MANE Select	NP_000438.2:n.*446T>C
NM_012486.3:c.*446T>C	NP_036618.2:n.*446T>C