Canonical Allele Identifier: CA345044544

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227083124G>T (hg19) ; chr1:g.226895423G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226895423G>T , CM000663.2:g.226895423G>T	GRCh38
NC_000001.10:g.227083124G>T , CM000663.1:g.227083124G>T	GRCh37
NC_000001.9:g.225149747G>T	NCBI36
NG_007381.1:g.29852G>T
NG_012825.2:g.2888G>T
NG_007381.2:g.30240G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366779.6:c.1192-1G>T	ENSP00000355741.2:n.1192-1G>T
ENST00000366782.6:c.1192-1G>T	ENSP00000355746.2:n.1192-1G>T
ENST00000366783.8:c.1192-1G>T MANE Select	ENSP00000355747.3:n.1192-1G>T
ENST00000471728.2:n.1830-1G>T
ENST00000524196.6:c.1192-1G>T	ENSP00000429036.2:n.1192-1G>T
ENST00000626989.3:c.1192-1G>T	ENSP00000486498.2:n.1192-1G>T
ENST00000676467.1:c.*1019-1G>T	ENSP00000504294.1:n.*1019-1G>T
ENST00000676747.1:c.1188+1298G>T	ENSP00000503244.1:n.1188+1298G>T
ENST00000676884.1:c.1192-1G>T	ENSP00000503200.1:n.1192-1G>T
ENST00000676888.1:c.*533-1G>T	ENSP00000504483.1:n.*533-1G>T
ENST00000676907.1:c.*771-1G>T	ENSP00000504410.1:n.*771-1G>T
ENST00000676945.1:c.1191+1298G>T	ENSP00000504433.1:n.1191+1298G>T
ENST00000677065.1:n.1753-1G>T
ENST00000677414.1:c.1192-1G>T	ENSP00000503116.1:n.1192-1G>T
ENST00000677529.1:n.2922-1G>T
ENST00000677596.1:c.*1414-1G>T	ENSP00000503618.1:n.*1414-1G>T
ENST00000677599.1:c.1191+1298G>T	ENSP00000503673.1:n.1191+1298G>T
ENST00000677748.1:n.3447-1G>T
ENST00000677880.1:c.757-1G>T	ENSP00000503121.1:n.757-1G>T
ENST00000678021.1:c.*815-1G>T	ENSP00000504674.1:n.*815-1G>T
ENST00000678233.1:c.1192-1G>T	ENSP00000504728.1:n.1192-1G>T
ENST00000678320.1:c.1093-1G>T	ENSP00000503680.1:n.1093-1G>T
ENST00000678655.1:c.1092+1298G>T	ENSP00000504230.1:n.1092+1298G>T
ENST00000678706.1:c.*569-1G>T	ENSP00000503659.1:n.*569-1G>T
ENST00000678776.1:c.*1329-1G>T	ENSP00000504624.1:n.*1329-1G>T
ENST00000678784.1:c.1073-2297G>T	ENSP00000504652.1:n.1073-2297G>T
ENST00000678820.1:c.1089+1298G>T	ENSP00000504138.1:n.1089+1298G>T
ENST00000678835.1:c.*757-2297G>T	ENSP00000504343.1:n.*757-2297G>T
ENST00000679088.1:c.1192-1G>T	ENSP00000504727.1:n.1192-1G>T
ENST00000679098.1:c.1192-1G>T	ENSP00000504303.1:n.1192-1G>T
ENST00000366782.5:c.1291-1G>T	ENSP00000355746.1:n.1291-1G>T
ENST00000366783.7:c.1192-1G>T	ENSP00000355747.3:n.1192-1G>T
ENST00000422240.6:c.1189-1G>T	ENSP00000403737.2:n.1189-1G>T
ENST00000471728.1:n.450-1G>T
ENST00000472139.2:c.760-1G>T	ENSP00000427806.1:n.760-1G>T
ENST00000626989.2:c.1291-1G>T	ENSP00000486498.1:n.1291-1G>T
NM_000447.2:c.1192-1G>T	NP_000438.2:n.1192-1G>T
NM_012486.2:c.1189-1G>T	NP_036618.2:n.1189-1G>T
XM_005273199.2:c.1192-1G>T	XP_005273256.1:n.1192-1G>T
XM_011544236.1:c.760-1G>T	XP_011542538.1:n.760-1G>T
XR_949149.1:n.1926-1G>T
XM_005273199.4:c.1192-1G>T	XP_005273256.1:n.1192-1G>T
XM_017001835.1:c.1192-1G>T	XP_016857324.1:n.1192-1G>T
XM_017001836.1:c.1189-1G>T	XP_016857325.1:n.1189-1G>T
XR_001737316.2:n.1478-2297G>T
XR_001737317.2:n.1478-2297G>T
XR_001737318.2:n.1907-1G>T
XR_001737319.1:n.2250-1G>T
XR_001737320.1:n.2247-1G>T
XR_001737321.1:n.1742-1G>T
XR_949149.2:n.1904-1G>T
XR_949150.3:n.2123-1G>T
NM_000447.3:c.1192-1G>T MANE Select	NP_000438.2:n.1192-1G>T
NM_012486.3:c.1189-1G>T	NP_036618.2:n.1189-1G>T