Canonical Allele Identifier: CA345040959

Gene: PSEN2

Linked Data

• dbSNP Id: rs1661558097
• MyVariant Identifiers: chr1:g.227076715C>T (hg19) ; chr1:g.226889014C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226889014C>T , CM000663.2:g.226889014C>T	GRCh38
NC_000001.10:g.227076715C>T , CM000663.1:g.227076715C>T	GRCh37
NC_000001.9:g.225143338C>T	NCBI36
NG_007381.1:g.23443C>T
NG_007381.2:g.23831C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366779.6:c.752C>T	ENSP00000355741.2:p.Ser251Phe
ENST00000366782.6:c.752C>T	ENSP00000355746.2:p.Ser251Phe
ENST00000366783.8:c.752C>T MANE Select	ENSP00000355747.3:p.Ser251Phe
ENST00000524196.6:c.752C>T	ENSP00000429036.2:p.Ser251Phe
ENST00000626989.3:c.752C>T	ENSP00000486498.2:p.Ser251Phe
ENST00000676467.1:c.*582C>T	ENSP00000504294.1:n.*582C>T
ENST00000676747.1:c.752C>T	ENSP00000503244.1:p.Ser251Phe
ENST00000676840.1:c.752C>T	ENSP00000504318.1:p.Ser251Phe
ENST00000676884.1:c.752C>T	ENSP00000503200.1:p.Ser251Phe
ENST00000676888.1:c.752C>T	ENSP00000504483.1:p.Ser251Phe
ENST00000676907.1:c.*331C>T	ENSP00000504410.1:n.*331C>T
ENST00000676945.1:c.752C>T	ENSP00000504433.1:p.Ser251Phe
ENST00000677065.1:n.1313C>T
ENST00000677414.1:c.752C>T	ENSP00000503116.1:p.Ser251Phe
ENST00000677529.1:n.1190C>T
ENST00000677596.1:c.*659C>T	ENSP00000503618.1:n.*659C>T
ENST00000677599.1:c.752C>T	ENSP00000503673.1:p.Ser251Phe
ENST00000677748.1:n.1190C>T
ENST00000677880.1:c.320C>T	ENSP00000503121.1:p.Ser107Phe
ENST00000678021.1:c.*375C>T	ENSP00000504674.1:n.*375C>T
ENST00000678233.1:c.752C>T	ENSP00000504728.1:p.Ser251Phe
ENST00000678320.1:c.752C>T	ENSP00000503680.1:p.Ser251Phe
ENST00000678655.1:c.752C>T	ENSP00000504230.1:p.Ser251Phe
ENST00000678706.1:c.752C>T	ENSP00000503659.1:p.Ser251Phe
ENST00000678776.1:c.*582C>T	ENSP00000504624.1:n.*582C>T
ENST00000678784.1:c.752C>T	ENSP00000504652.1:p.Ser251Phe
ENST00000678820.1:c.752C>T	ENSP00000504138.1:p.Ser251Phe
ENST00000678835.1:c.752C>T	ENSP00000504343.1:p.Ser251Phe
ENST00000679088.1:c.752C>T	ENSP00000504727.1:p.Ser251Phe
ENST00000679098.1:c.752C>T	ENSP00000504303.1:p.Ser251Phe
ENST00000366782.5:c.851C>T	ENSP00000355746.1:p.Ser284Phe
ENST00000366783.7:c.752C>T	ENSP00000355747.3:p.Ser251Phe
ENST00000422240.6:c.752C>T	ENSP00000403737.2:p.Ser251Phe
ENST00000460775.5:c.233C>T	ENSP00000427912.1:p.Ser78Phe
ENST00000472139.2:c.320C>T	ENSP00000427806.1:p.Ser107Phe
ENST00000626989.2:c.851C>T	ENSP00000486498.1:p.Ser284Phe
NM_000447.2:c.752C>T	NP_000438.2:p.Ser251Phe
NM_012486.2:c.752C>T	NP_036618.2:p.Ser251Phe
XM_005273199.2:c.752C>T	XP_005273256.1:p.Ser251Phe
XM_011544236.1:c.320C>T	XP_011542538.1:p.Ser107Phe
XR_949149.1:n.1179C>T
XR_949150.1:n.1179C>T
XM_005273199.4:c.752C>T	XP_005273256.1:p.Ser251Phe
XM_017001835.1:c.752C>T	XP_016857324.1:p.Ser251Phe
XM_017001836.1:c.752C>T	XP_016857325.1:p.Ser251Phe
XR_001737316.2:n.1157C>T
XR_001737317.2:n.1157C>T
XR_001737318.2:n.1157C>T
XR_001737319.1:n.1500C>T
XR_001737320.1:n.1500C>T
XR_001737321.1:n.992C>T
XR_949149.2:n.1157C>T
XR_949150.3:n.1157C>T
NM_000447.3:c.752C>T MANE Select	NP_000438.2:p.Ser251Phe
NM_012486.3:c.752C>T	NP_036618.2:p.Ser251Phe