Canonical Allele Identifier: CA345043986

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227081753T>G (hg19) ; chr1:g.226894052T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226894052T>G , CM000663.2:g.226894052T>G	GRCh38
NC_000001.10:g.227081753T>G , CM000663.1:g.227081753T>G	GRCh37
NC_000001.9:g.225148376T>G	NCBI36
NG_007381.1:g.28481T>G
NG_012825.2:g.1517T>G
NG_007381.2:g.28869T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.1118T>G	ENSP00000355741.2:p.Leu373Arg
ENST00000366782.6:c.1118T>G	ENSP00000355746.2:p.Leu373Arg
ENST00000366783.8:c.1118T>G MANE Select	ENSP00000355747.3:p.Leu373Arg
ENST00000471728.2:n.1756T>G
ENST00000524196.6:c.1118T>G	ENSP00000429036.2:p.Leu373Arg
ENST00000626989.3:c.1118T>G	ENSP00000486498.2:p.Leu373Arg
ENST00000676467.1:c.*945T>G	ENSP00000504294.1:n.*945T>G
ENST00000676747.1:c.1115T>G	ENSP00000503244.1:p.Leu372Arg
ENST00000676884.1:c.1118T>G	ENSP00000503200.1:p.Leu373Arg
ENST00000676888.1:c.*459T>G	ENSP00000504483.1:n.*459T>G
ENST00000676907.1:c.*697T>G	ENSP00000504410.1:n.*697T>G
ENST00000676945.1:c.1118T>G	ENSP00000504433.1:p.Leu373Arg
ENST00000677065.1:n.1679T>G
ENST00000677414.1:c.1118T>G	ENSP00000503116.1:p.Leu373Arg
ENST00000677529.1:n.2848T>G
ENST00000677596.1:c.*1340T>G	ENSP00000503618.1:n.*1340T>G
ENST00000677599.1:c.1118T>G	ENSP00000503673.1:p.Leu373Arg
ENST00000677748.1:n.3373T>G
ENST00000677880.1:c.683T>G	ENSP00000503121.1:p.Leu228Arg
ENST00000678021.1:c.*741T>G	ENSP00000504674.1:n.*741T>G
ENST00000678233.1:c.1118T>G	ENSP00000504728.1:p.Leu373Arg
ENST00000678320.1:c.1019T>G	ENSP00000503680.1:p.Leu340Arg
ENST00000678655.1:c.1019T>G	ENSP00000504230.1:p.Leu340Arg
ENST00000678706.1:c.*495T>G	ENSP00000503659.1:n.*495T>G
ENST00000678776.1:c.*1255T>G	ENSP00000504624.1:n.*1255T>G
ENST00000678784.1:c.1072+2208T>G	ENSP00000504652.1:n.1072+2208T>G
ENST00000678820.1:c.1016T>G	ENSP00000504138.1:p.Leu339Arg
ENST00000678835.1:c.*756+2208T>G	ENSP00000504343.1:n.*756+2208T>G
ENST00000679088.1:c.1118T>G	ENSP00000504727.1:p.Leu373Arg
ENST00000679098.1:c.1118T>G	ENSP00000504303.1:p.Leu373Arg
ENST00000366782.5:c.1217T>G	ENSP00000355746.1:p.Leu406Arg
ENST00000366783.7:c.1118T>G	ENSP00000355747.3:p.Leu373Arg
ENST00000422240.6:c.1115T>G	ENSP00000403737.2:p.Leu372Arg
ENST00000471728.1:n.376T>G
ENST00000472139.2:c.686T>G	ENSP00000427806.1:p.Leu229Arg
ENST00000626989.2:c.1217T>G	ENSP00000486498.1:p.Leu406Arg
NM_000447.2:c.1118T>G	NP_000438.2:p.Leu373Arg
NM_012486.2:c.1115T>G	NP_036618.2:p.Leu372Arg
XM_005273199.2:c.1118T>G	XP_005273256.1:p.Leu373Arg
XM_011544236.1:c.686T>G	XP_011542538.1:p.Leu229Arg
XR_949149.1:n.1852T>G
XM_005273199.4:c.1118T>G	XP_005273256.1:p.Leu373Arg
XM_017001835.1:c.1118T>G	XP_016857324.1:p.Leu373Arg
XM_017001836.1:c.1115T>G	XP_016857325.1:p.Leu372Arg
XR_001737316.2:n.1477+2208T>G
XR_001737317.2:n.1477+2208T>G
XR_001737318.2:n.1833T>G
XR_001737319.1:n.2176T>G
XR_001737320.1:n.2173T>G
XR_001737321.1:n.1668T>G
XR_949149.2:n.1830T>G
XR_949150.3:n.2049T>G
NM_000447.3:c.1118T>G MANE Select	NP_000438.2:p.Leu373Arg
NM_012486.3:c.1115T>G	NP_036618.2:p.Leu372Arg