Canonical Allele Identifier: CA262615135
Gene: PSEN1 HGNC NCBI

Linked Data

dbSNP Id: rs899821281

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73173526T>G , CM000676.2:g.73173526T>G GRCh38
NC_000014.8:g.73640234T>G , CM000676.1:g.73640234T>G GRCh37
NC_000014.7:g.72709987T>G NCBI36
NG_007386.2:g.42056T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000324501.10:c.339-40T>G MANE Select ENSP00000326366.5:n.339-40T>G
ENST00000324501.9:c.339-40T>G ENSP00000326366.5:n.339-40T>G
ENST00000357710.8:c.327-40T>G ENSP00000350342.4:n.327-40T>G
ENST00000394157.7:c.339-40T>G ENSP00000377712.3:n.339-40T>G
ENST00000394164.5:c.327-40T>G ENSP00000377719.1:n.327-40T>G
ENST00000406768.1:c.63-40T>G ENSP00000385948.1:n.63-40T>G
ENST00000553719.5:c.327-40T>G ENSP00000451674.1:n.327-40T>G
ENST00000553855.5:n.339-40T>G ENSP00000452242.1:n.339-40T>G
ENST00000555254.5:c.339-40T>G ENSP00000450652.1:n.339-40T>G
ENST00000555386.5:n.327-40T>G ENSP00000450845.1:n.327-40T>G
ENST00000557356.5:c.327-40T>G ENSP00000451498.1:n.327-40T>G
ENST00000557511.5:n.339-40T>G ENSP00000451429.1:n.339-40T>G
ENST00000559361.5:c.*283-40T>G ENSP00000454156.1:n.*283-40T>G
NM_000021.3:c.339-40T>G NP_000012.1:n.339-40T>G
NM_007318.2:c.327-40T>G NP_015557.2:n.327-40T>G
XM_005267864.1:c.339-40T>G XP_005267921.1:n.339-40T>G
XM_005267866.1:c.327-40T>G XP_005267923.1:n.327-40T>G
XM_011536971.1:c.339-40T>G XP_011535273.1:n.339-40T>G
XM_011536972.1:c.339-40T>G XP_011535274.1:n.339-40T>G
XM_011536973.1:c.327-40T>G XP_011535275.1:n.327-40T>G
XM_011536974.1:c.327-40T>G XP_011535276.1:n.327-40T>G
XM_005267864.3:c.339-40T>G XP_005267921.1:n.339-40T>G
XM_005267866.2:c.327-40T>G XP_005267923.1:n.327-40T>G
XM_011536972.2:c.339-40T>G XP_011535274.1:n.339-40T>G
XM_011536973.2:c.327-40T>G XP_011535275.1:n.327-40T>G
XM_011536974.2:c.327-40T>G XP_011535276.1:n.327-40T>G
NM_000021.4:c.339-40T>G MANE Select NP_000012.1:n.339-40T>G
NM_007318.3:c.327-40T>G NP_015557.2:n.327-40T>G