Canonical Allele Identifier: CA345040909

Gene: PSEN2

Linked Data

• MyVariant Identifiers: chr1:g.227076710G>T (hg19) ; chr1:g.226889009G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226889009G>T , CM000663.2:g.226889009G>T	GRCh38
NC_000001.10:g.227076710G>T , CM000663.1:g.227076710G>T	GRCh37
NC_000001.9:g.225143333G>T	NCBI36
NG_007381.1:g.23438G>T
NG_007381.2:g.23826G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000366779.6:c.747G>T	ENSP00000355741.2:p.Glu249Asp
ENST00000366782.6:c.747G>T	ENSP00000355746.2:p.Glu249Asp
ENST00000366783.8:c.747G>T MANE Select	ENSP00000355747.3:p.Glu249Asp
ENST00000524196.6:c.747G>T	ENSP00000429036.2:p.Glu249Asp
ENST00000626989.3:c.747G>T	ENSP00000486498.2:p.Glu249Asp
ENST00000676467.1:c.*577G>T	ENSP00000504294.1:n.*577G>T
ENST00000676747.1:c.747G>T	ENSP00000503244.1:p.Glu249Asp
ENST00000676840.1:c.747G>T	ENSP00000504318.1:p.Glu249Asp
ENST00000676884.1:c.747G>T	ENSP00000503200.1:p.Glu249Asp
ENST00000676888.1:c.747G>T	ENSP00000504483.1:p.Glu249Asp
ENST00000676907.1:c.*326G>T	ENSP00000504410.1:n.*326G>T
ENST00000676945.1:c.747G>T	ENSP00000504433.1:p.Glu249Asp
ENST00000677065.1:n.1308G>T
ENST00000677414.1:c.747G>T	ENSP00000503116.1:p.Glu249Asp
ENST00000677529.1:n.1185G>T
ENST00000677596.1:c.*654G>T	ENSP00000503618.1:n.*654G>T
ENST00000677599.1:c.747G>T	ENSP00000503673.1:p.Glu249Asp
ENST00000677748.1:n.1185G>T
ENST00000677880.1:c.315G>T	ENSP00000503121.1:p.Glu105Asp
ENST00000678021.1:c.*370G>T	ENSP00000504674.1:n.*370G>T
ENST00000678233.1:c.747G>T	ENSP00000504728.1:p.Glu249Asp
ENST00000678320.1:c.747G>T	ENSP00000503680.1:p.Glu249Asp
ENST00000678655.1:c.747G>T	ENSP00000504230.1:p.Glu249Asp
ENST00000678706.1:c.747G>T	ENSP00000503659.1:p.Glu249Asp
ENST00000678776.1:c.*577G>T	ENSP00000504624.1:n.*577G>T
ENST00000678784.1:c.747G>T	ENSP00000504652.1:p.Glu249Asp
ENST00000678820.1:c.747G>T	ENSP00000504138.1:p.Glu249Asp
ENST00000678835.1:c.747G>T	ENSP00000504343.1:p.Glu249Asp
ENST00000679088.1:c.747G>T	ENSP00000504727.1:p.Glu249Asp
ENST00000679098.1:c.747G>T	ENSP00000504303.1:p.Glu249Asp
ENST00000366782.5:c.846G>T	ENSP00000355746.1:p.Glu282Asp
ENST00000366783.7:c.747G>T	ENSP00000355747.3:p.Glu249Asp
ENST00000422240.6:c.747G>T	ENSP00000403737.2:p.Glu249Asp
ENST00000460775.5:c.228G>T	ENSP00000427912.1:p.Glu76Asp
ENST00000472139.2:c.315G>T	ENSP00000427806.1:p.Glu105Asp
ENST00000626989.2:c.846G>T	ENSP00000486498.1:p.Glu282Asp
NM_000447.2:c.747G>T	NP_000438.2:p.Glu249Asp
NM_012486.2:c.747G>T	NP_036618.2:p.Glu249Asp
XM_005273199.2:c.747G>T	XP_005273256.1:p.Glu249Asp
XM_011544236.1:c.315G>T	XP_011542538.1:p.Glu105Asp
XR_949149.1:n.1174G>T
XR_949150.1:n.1174G>T
XM_005273199.4:c.747G>T	XP_005273256.1:p.Glu249Asp
XM_017001835.1:c.747G>T	XP_016857324.1:p.Glu249Asp
XM_017001836.1:c.747G>T	XP_016857325.1:p.Glu249Asp
XR_001737316.2:n.1152G>T
XR_001737317.2:n.1152G>T
XR_001737318.2:n.1152G>T
XR_001737319.1:n.1495G>T
XR_001737320.1:n.1495G>T
XR_001737321.1:n.987G>T
XR_949149.2:n.1152G>T
XR_949150.3:n.1152G>T
NM_000447.3:c.747G>T MANE Select	NP_000438.2:p.Glu249Asp
NM_012486.3:c.747G>T	NP_036618.2:p.Glu249Asp