Canonical Allele Identifier: CA38625705

Gene: PSEN2

Linked Data

• dbSNP Id: rs1050696629
• gnomAD v3: 1-226894324-C-T
• gnomAD v4: 1-226894324-C-T
• MyVariant Identifiers: chr1:g.227082025C>T (hg19) ; chr1:g.226894324C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894324C>T , CM000663.2:g.226894324C>T	GRCh38
NC_000001.10:g.227082025C>T , CM000663.1:g.227082025C>T	GRCh37
NC_000001.9:g.225148648C>T	NCBI36
NG_007381.1:g.28753C>T
NG_012825.2:g.1789C>T
NG_007381.2:g.29141C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1191+199C>T	ENSP00000355741.2:n.1191+199C>T
ENST00000366782.6:c.1191+199C>T	ENSP00000355746.2:n.1191+199C>T
ENST00000366783.8:c.1191+199C>T MANE Select	ENSP00000355747.3:n.1191+199C>T
ENST00000471728.2:n.1829+199C>T
ENST00000524196.6:c.1191+199C>T	ENSP00000429036.2:n.1191+199C>T
ENST00000626989.3:c.1191+199C>T	ENSP00000486498.2:n.1191+199C>T
ENST00000676467.1:c.*1018+199C>T	ENSP00000504294.1:n.*1018+199C>T
ENST00000676747.1:c.1188+199C>T	ENSP00000503244.1:n.1188+199C>T
ENST00000676884.1:c.1191+199C>T	ENSP00000503200.1:n.1191+199C>T
ENST00000676888.1:c.*532+199C>T	ENSP00000504483.1:n.*532+199C>T
ENST00000676907.1:c.*770+199C>T	ENSP00000504410.1:n.*770+199C>T
ENST00000676945.1:c.1191+199C>T	ENSP00000504433.1:n.1191+199C>T
ENST00000677065.1:n.1752+199C>T
ENST00000677414.1:c.1191+199C>T	ENSP00000503116.1:n.1191+199C>T
ENST00000677529.1:n.2921+199C>T
ENST00000677596.1:c.*1413+199C>T	ENSP00000503618.1:n.*1413+199C>T
ENST00000677599.1:c.1191+199C>T	ENSP00000503673.1:n.1191+199C>T
ENST00000677748.1:n.3446+199C>T
ENST00000677880.1:c.756+199C>T	ENSP00000503121.1:n.756+199C>T
ENST00000678021.1:c.*814+199C>T	ENSP00000504674.1:n.*814+199C>T
ENST00000678233.1:c.1191+199C>T	ENSP00000504728.1:n.1191+199C>T
ENST00000678320.1:c.1092+199C>T	ENSP00000503680.1:n.1092+199C>T
ENST00000678655.1:c.1092+199C>T	ENSP00000504230.1:n.1092+199C>T
ENST00000678706.1:c.*568+199C>T	ENSP00000503659.1:n.*568+199C>T
ENST00000678776.1:c.*1328+199C>T	ENSP00000504624.1:n.*1328+199C>T
ENST00000678784.1:c.1072+2480C>T	ENSP00000504652.1:n.1072+2480C>T
ENST00000678820.1:c.1089+199C>T	ENSP00000504138.1:n.1089+199C>T
ENST00000678835.1:c.*756+2480C>T	ENSP00000504343.1:n.*756+2480C>T
ENST00000679088.1:c.1191+199C>T	ENSP00000504727.1:n.1191+199C>T
ENST00000679098.1:c.1191+199C>T	ENSP00000504303.1:n.1191+199C>T
ENST00000366782.5:c.1290+199C>T	ENSP00000355746.1:n.1290+199C>T
ENST00000366783.7:c.1191+199C>T	ENSP00000355747.3:n.1191+199C>T
ENST00000422240.6:c.1188+199C>T	ENSP00000403737.2:n.1188+199C>T
ENST00000471728.1:n.449+199C>T
ENST00000472139.2:c.759+199C>T	ENSP00000427806.1:n.759+199C>T
ENST00000626989.2:c.1290+199C>T	ENSP00000486498.1:n.1290+199C>T
NM_000447.2:c.1191+199C>T	NP_000438.2:n.1191+199C>T
NM_012486.2:c.1188+199C>T	NP_036618.2:n.1188+199C>T
XM_005273199.2:c.1191+199C>T	XP_005273256.1:n.1191+199C>T
XM_011544236.1:c.759+199C>T	XP_011542538.1:n.759+199C>T
XR_949149.1:n.1925+199C>T
XM_005273199.4:c.1191+199C>T	XP_005273256.1:n.1191+199C>T
XM_017001835.1:c.1191+199C>T	XP_016857324.1:n.1191+199C>T
XM_017001836.1:c.1188+199C>T	XP_016857325.1:n.1188+199C>T
XR_001737316.2:n.1477+2480C>T
XR_001737317.2:n.1477+2480C>T
XR_001737318.2:n.1906+199C>T
XR_001737319.1:n.2249+199C>T
XR_001737320.1:n.2246+199C>T
XR_001737321.1:n.1741+199C>T
XR_949149.2:n.1903+199C>T
XR_949150.3:n.2122+199C>T
NM_000447.3:c.1191+199C>T MANE Select	NP_000438.2:n.1191+199C>T
NM_012486.3:c.1188+199C>T	NP_036618.2:n.1188+199C>T