Canonical Allele Identifier: CA708407743
Gene: PSEN1 HGNC NCBI

Linked Data

dbSNP Id: rs1329970389

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73173504_73173505insGGGTGG , CM000676.2:g.73173504_73173505insGGGTGG GRCh38
NC_000014.8:g.73640212_73640213insGGGTGG , CM000676.1:g.73640212_73640213insGGGTGG GRCh37
NC_000014.7:g.72709965_72709966insGGGTGG NCBI36
NG_007386.2:g.42034_42035insGGGTGG

Transcript Alleles

HGVS Amino-acid change
ENST00000324501.10:c.339-62_339-61insGGGTGG MANE Select ENSP00000326366.5:n.339-62_339-61insGGGTG...
ENST00000324501.9:c.339-62_339-61insGGGTGG ENSP00000326366.5:n.339-62_339-61insGGGTG...
ENST00000357710.8:c.327-62_327-61insGGGTGG ENSP00000350342.4:n.327-62_327-61insGGGTG...
ENST00000394157.7:c.339-62_339-61insGGGTGG ENSP00000377712.3:n.339-62_339-61insGGGTG...
ENST00000394164.5:c.327-62_327-61insGGGTGG ENSP00000377719.1:n.327-62_327-61insGGGTG...
ENST00000406768.1:c.63-62_63-61insGGGTGG ENSP00000385948.1:n.63-62_63-61insGGGTGG
ENST00000553719.5:c.327-62_327-61insGGGTGG ENSP00000451674.1:n.327-62_327-61insGGGTG...
ENST00000553855.5:n.339-62_339-61insGGGTGG ENSP00000452242.1:n.339-62_339-61insGGGTG...
ENST00000555254.5:c.339-62_339-61insGGGTGG ENSP00000450652.1:n.339-62_339-61insGGGTG...
ENST00000555386.5:n.327-62_327-61insGGGTGG ENSP00000450845.1:n.327-62_327-61insGGGTG...
ENST00000557356.5:c.327-62_327-61insGGGTGG ENSP00000451498.1:n.327-62_327-61insGGGTG...
ENST00000557511.5:n.339-62_339-61insGGGTGG ENSP00000451429.1:n.339-62_339-61insGGGTG...
ENST00000559361.5:c.*283-62_*283-61insGGGTGG ENSP00000454156.1:n.*283-62_*283-61insGGG...
NM_000021.3:c.339-62_339-61insGGGTGG NP_000012.1:n.339-62_339-61insGGGTGG
NM_007318.2:c.327-62_327-61insGGGTGG NP_015557.2:n.327-62_327-61insGGGTGG
XM_005267864.1:c.339-62_339-61insGGGTGG XP_005267921.1:n.339-62_339-61insGGGTGG
XM_005267866.1:c.327-62_327-61insGGGTGG XP_005267923.1:n.327-62_327-61insGGGTGG
XM_011536971.1:c.339-62_339-61insGGGTGG XP_011535273.1:n.339-62_339-61insGGGTGG
XM_011536972.1:c.339-62_339-61insGGGTGG XP_011535274.1:n.339-62_339-61insGGGTGG
XM_011536973.1:c.327-62_327-61insGGGTGG XP_011535275.1:n.327-62_327-61insGGGTGG
XM_011536974.1:c.327-62_327-61insGGGTGG XP_011535276.1:n.327-62_327-61insGGGTGG
XM_005267864.3:c.339-62_339-61insGGGTGG XP_005267921.1:n.339-62_339-61insGGGTGG
XM_005267866.2:c.327-62_327-61insGGGTGG XP_005267923.1:n.327-62_327-61insGGGTGG
XM_011536972.2:c.339-62_339-61insGGGTGG XP_011535274.1:n.339-62_339-61insGGGTGG
XM_011536973.2:c.327-62_327-61insGGGTGG XP_011535275.1:n.327-62_327-61insGGGTGG
XM_011536974.2:c.327-62_327-61insGGGTGG XP_011535276.1:n.327-62_327-61insGGGTGG
NM_000021.4:c.339-62_339-61insGGGTGG MANE Select NP_000012.1:n.339-62_339-61insGGGTGG
NM_007318.3:c.327-62_327-61insGGGTGG NP_015557.2:n.327-62_327-61insGGGTGG