Canonical Allele Identifier: CA390303014
Gene: PSEN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73170926C>G , CM000676.2:g.73170926C>G GRCh38
NC_000014.8:g.73637634C>G , CM000676.1:g.73637634C>G GRCh37
NC_000014.7:g.72707387C>G NCBI36
NG_007386.2:g.39456C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000324501.10:c.217C>G MANE Select ENSP00000326366.5:p.Leu73Val
ENST00000324501.9:c.217C>G ENSP00000326366.5:p.Leu73Val
ENST00000357710.8:c.205C>G ENSP00000350342.4:p.Leu69Val
ENST00000394157.7:c.217C>G ENSP00000377712.3:p.Leu73Val
ENST00000394164.5:c.205C>G ENSP00000377719.1:p.Leu69Val
ENST00000406768.1:c.-60C>G ENSP00000385948.1:n.-60C>G
ENST00000553599.5:c.205C>G ENSP00000452477.1:p.Leu69Val
ENST00000553719.5:c.205C>G ENSP00000451674.1:p.Leu69Val
ENST00000553855.5:n.217C>G ENSP00000452242.1:p.Leu73Val
ENST00000554131.5:c.217C>G ENSP00000451915.1:p.Leu73Val
ENST00000555254.5:c.217C>G ENSP00000450652.1:p.Leu73Val
ENST00000555386.5:n.205C>G ENSP00000450845.1:p.Leu69Val
ENST00000556533.5:c.205C>G ENSP00000452128.1:p.Leu69Val
ENST00000556951.5:c.205C>G ENSP00000450551.1:p.Leu69Val
ENST00000557293.5:c.217C>G ENSP00000451880.1:p.Leu73Val
ENST00000557356.5:c.205C>G ENSP00000451498.1:p.Leu69Val
ENST00000557511.5:n.217C>G ENSP00000451429.1:p.Leu73Val
ENST00000559361.5:c.*161C>G ENSP00000454156.1:n.*161C>G
ENST00000560005.6:c.205C>G ENSP00000453466.1:p.Leu69Val
NM_000021.3:c.217C>G NP_000012.1:p.Leu73Val
NM_007318.2:c.205C>G NP_015557.2:p.Leu69Val
XM_005267864.1:c.217C>G XP_005267921.1:p.Leu73Val
XM_005267866.1:c.205C>G XP_005267923.1:p.Leu69Val
XM_011536971.1:c.217C>G XP_011535273.1:p.Leu73Val
XM_011536972.1:c.217C>G XP_011535274.1:p.Leu73Val
XM_011536973.1:c.205C>G XP_011535275.1:p.Leu69Val
XM_011536974.1:c.205C>G XP_011535276.1:p.Leu69Val
XM_005267864.3:c.217C>G XP_005267921.1:p.Leu73Val
XM_005267866.2:c.205C>G XP_005267923.1:p.Leu69Val
XM_011536972.2:c.217C>G XP_011535274.1:p.Leu73Val
XM_011536973.2:c.205C>G XP_011535275.1:p.Leu69Val
XM_011536974.2:c.205C>G XP_011535276.1:p.Leu69Val
NM_000021.4:c.217C>G MANE Select NP_000012.1:p.Leu73Val
NM_007318.3:c.205C>G NP_015557.2:p.Leu69Val