Canonical Allele Identifier: CA2625553113
Gene: PSEN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73136446A>G , CM000676.2:g.73136446A>G GRCh38
NC_000014.8:g.73603154A>G , CM000676.1:g.73603154A>G GRCh37
NC_000014.7:g.72672907A>G NCBI36
NG_007386.2:g.4976A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000553599.6:c.-315A>G ENSP00000452477.2:n.-315A>G
ENST00000556951.6:c.-269A>G ENSP00000450551.2:n.-269A>G
ENST00000557293.6:c.-269A>G ENSP00000451880.2:n.-269A>G
ENST00000700265.1:c.-106A>G ENSP00000514901.1:n.-106A>G
ENST00000700266.1:c.-273A>G ENSP00000514902.1:n.-273A>G
ENST00000700267.1:c.-138A>G ENSP00000514903.1:n.-138A>G
ENST00000700268.1:c.-269A>G ENSP00000514904.1:n.-269A>G
ENST00000700269.1:c.-315A>G ENSP00000514905.1:n.-315A>G
ENST00000553599.5:c.-315A>G ENSP00000452477.1:n.-315A>G
ENST00000553719.5:c.-269A>G ENSP00000451674.1:n.-269A>G
ENST00000556533.5:c.-262A>G ENSP00000452128.1:n.-262A>G
ENST00000556864.5:c.-372A>G ENSP00000451588.1:n.-372A>G
ENST00000556951.5:c.-269A>G ENSP00000450551.1:n.-269A>G
ENST00000557293.5:c.-269A>G ENSP00000451880.1:n.-269A>G
ENST00000557356.5:c.-138A>G ENSP00000451498.1:n.-138A>G
NM_000021.3:c.-273A>G NP_000012.1:n.-273A>G
NM_007318.2:c.-273A>G NP_015557.2:n.-273A>G
XM_005267864.1:c.-269A>G XP_005267921.1:n.-269A>G
XM_005267866.1:c.-269A>G XP_005267923.1:n.-269A>G
XM_005267864.3:c.-269A>G XP_005267921.1:n.-269A>G
XM_005267866.2:c.-269A>G XP_005267923.1:n.-269A>G