Canonical Allele Identifier: CA423660646

Gene: PSEN2

Linked Data

• gnomAD v4: 1-226885538-C-T
• COSMIC: COSM6061669 ; COSM6061670
• MyVariant Identifiers: chr1:g.227073239C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.226885538C>T , CM000663.2:g.226885538C>T	GRCh38
NC_000001.10:g.227073239C>T , CM000663.1:g.227073239C>T	GRCh37
NC_000001.9:g.225139862C>T	NCBI36
NG_007381.1:g.19967C>T
NG_007381.2:g.20355C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000366779.6:c.357C>T	ENSP00000355741.2:p.Leu119=
ENST00000366782.6:c.357C>T	ENSP00000355746.2:p.Leu119=
ENST00000366783.8:c.357C>T MANE Select	ENSP00000355747.3:p.Leu119=
ENST00000524196.6:c.357C>T	ENSP00000429036.2:p.Leu119=
ENST00000626989.3:c.357C>T	ENSP00000486498.2:p.Leu119=
ENST00000676467.1:c.*187C>T	ENSP00000504294.1:n.*187C>T
ENST00000676747.1:c.357C>T	ENSP00000503244.1:p.Leu119=
ENST00000676840.1:c.357C>T	ENSP00000504318.1:p.Leu119=
ENST00000676884.1:c.357C>T	ENSP00000503200.1:p.Leu119=
ENST00000676888.1:c.357C>T	ENSP00000504483.1:p.Leu119=
ENST00000676907.1:c.434C>T	ENSP00000504410.1:p.Ala145Val
ENST00000676945.1:c.357C>T	ENSP00000504433.1:p.Leu119=
ENST00000677065.1:n.918C>T
ENST00000677414.1:c.357C>T	ENSP00000503116.1:p.Leu119=
ENST00000677529.1:n.795C>T
ENST00000677596.1:c.*264C>T	ENSP00000503618.1:n.*264C>T
ENST00000677599.1:c.357C>T	ENSP00000503673.1:p.Leu119=
ENST00000677748.1:n.795C>T
ENST00000677880.1:c.-76C>T	ENSP00000503121.1:n.-76C>T
ENST00000678021.1:c.142C>T	ENSP00000504674.1:p.His48Tyr
ENST00000678233.1:c.357C>T	ENSP00000504728.1:p.Leu119=
ENST00000678320.1:c.357C>T	ENSP00000503680.1:p.Leu119=
ENST00000678655.1:c.357C>T	ENSP00000504230.1:p.Leu119=
ENST00000678706.1:c.357C>T	ENSP00000503659.1:p.Leu119=
ENST00000678776.1:c.*187C>T	ENSP00000504624.1:n.*187C>T
ENST00000678784.1:c.357C>T	ENSP00000504652.1:p.Leu119=
ENST00000678820.1:c.357C>T	ENSP00000504138.1:p.Leu119=
ENST00000678835.1:c.357C>T	ENSP00000504343.1:p.Leu119=
ENST00000679088.1:c.357C>T	ENSP00000504727.1:p.Leu119=
ENST00000679098.1:c.357C>T	ENSP00000504303.1:p.Leu119=
ENST00000366782.5:c.456C>T	ENSP00000355746.1:p.Leu152=
ENST00000366783.7:c.357C>T	ENSP00000355747.3:p.Leu119=
ENST00000422240.6:c.357C>T	ENSP00000403737.2:p.Leu119=
ENST00000460775.5:c.-21-2553C>T	ENSP00000427912.1:n.-21-2553C>T
ENST00000472139.2:c.-76C>T	ENSP00000427806.1:n.-76C>T
ENST00000495488.5:c.357C>T	ENSP00000429682.1:p.Leu119=
ENST00000626989.2:c.456C>T	ENSP00000486498.1:p.Leu152=
NM_000447.2:c.357C>T	NP_000438.2:p.Leu119=
NM_012486.2:c.357C>T	NP_036618.2:p.Leu119=
XM_005273199.2:c.357C>T	XP_005273256.1:p.Leu119=
XM_011544236.1:c.-76C>T	XP_011542538.1:n.-76C>T
XR_949149.1:n.784C>T
XR_949150.1:n.784C>T
XM_005273199.4:c.357C>T	XP_005273256.1:p.Leu119=
XM_017001835.1:c.357C>T	XP_016857324.1:p.Leu119=
XM_017001836.1:c.357C>T	XP_016857325.1:p.Leu119=
XR_001737316.2:n.762C>T
XR_001737317.2:n.762C>T
XR_001737318.2:n.762C>T
XR_001737319.1:n.1105C>T
XR_001737320.1:n.1105C>T
XR_001737321.1:n.597C>T
XR_949149.2:n.762C>T
XR_949150.3:n.762C>T
NM_000447.3:c.357C>T MANE Select	NP_000438.2:p.Leu119=
NM_012486.3:c.357C>T	NP_036618.2:p.Leu119=