Canonical Allele Identifier: CA262598412
Gene: PSEN1 HGNC NCBI

Linked Data

dbSNP Id: rs201092260

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73136449G>A , CM000676.2:g.73136449G>A GRCh38
NC_000014.8:g.73603157G>A , CM000676.1:g.73603157G>A GRCh37
NC_000014.7:g.72672910G>A NCBI36
NG_007386.2:g.4979G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000553599.6:c.-312G>A ENSP00000452477.2:n.-312G>A
ENST00000556011.6:c.-312G>A ENSP00000451662.2:n.-312G>A
ENST00000556951.6:c.-266G>A ENSP00000450551.2:n.-266G>A
ENST00000557293.6:c.-266G>A ENSP00000451880.2:n.-266G>A
ENST00000700265.1:c.-104+1G>A ENSP00000514901.1:n.-104+1G>A
ENST00000700266.1:c.-270G>A ENSP00000514902.1:n.-270G>A
ENST00000700267.1:c.-136+1G>A ENSP00000514903.1:n.-136+1G>A
ENST00000700268.1:c.-266G>A ENSP00000514904.1:n.-266G>A
ENST00000700269.1:c.-312G>A ENSP00000514905.1:n.-312G>A
ENST00000324501.9:c.-270G>A ENSP00000326366.5:n.-270G>A
ENST00000357710.8:c.-270G>A ENSP00000350342.4:n.-270G>A
ENST00000394157.7:c.-270G>A ENSP00000377712.3:n.-270G>A
ENST00000553599.5:c.-312G>A ENSP00000452477.1:n.-312G>A
ENST00000553719.5:c.-266G>A ENSP00000451674.1:n.-266G>A
ENST00000556011.5:c.-312G>A ENSP00000451662.1:n.-312G>A
ENST00000556533.5:c.-259G>A ENSP00000452128.1:n.-259G>A
ENST00000556864.5:c.-369G>A ENSP00000451588.1:n.-369G>A
ENST00000556951.5:c.-266G>A ENSP00000450551.1:n.-266G>A
ENST00000557293.5:c.-266G>A ENSP00000451880.1:n.-266G>A
ENST00000557356.5:c.-136+1G>A ENSP00000451498.1:n.-136+1G>A
NM_000021.3:c.-270G>A NP_000012.1:n.-270G>A
NM_007318.2:c.-270G>A NP_015557.2:n.-270G>A
XM_005267864.1:c.-266G>A XP_005267921.1:n.-266G>A
XM_005267866.1:c.-266G>A XP_005267923.1:n.-266G>A
XM_005267864.3:c.-266G>A XP_005267921.1:n.-266G>A
XM_005267866.2:c.-266G>A XP_005267923.1:n.-266G>A