Canonical Allele Identifier: CA2146453831
Gene: PSEN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73136437A= , CM000676.2:g.73136437A= GRCh38
NC_000014.8:g.73603145A= , CM000676.1:g.73603145A= GRCh37
NC_000014.7:g.72672898A= NCBI36
NG_007386.2:g.4967A=

Transcript Alleles

HGVS Amino-acid change
ENST00000556951.6:c.-278A= ENSP00000450551.2:n.-278A=
ENST00000557293.6:c.-278A= ENSP00000451880.2:n.-278A=
ENST00000700265.1:c.-115A= ENSP00000514901.1:n.-115A=
ENST00000700266.1:c.-282A= ENSP00000514902.1:n.-282A=
ENST00000700267.1:c.-147A= ENSP00000514903.1:n.-147A=
ENST00000556533.5:c.-271A= ENSP00000452128.1:n.-271A=
ENST00000556864.5:c.-381A= ENSP00000451588.1:n.-381A=
ENST00000556951.5:c.-278A= ENSP00000450551.1:n.-278A=
ENST00000557293.5:c.-278A= ENSP00000451880.1:n.-278A=
ENST00000557356.5:c.-147A= ENSP00000451498.1:n.-147A=
NM_000021.3:c.-282A= NP_000012.1:n.-282A=
NM_007318.2:c.-282A= NP_015557.2:n.-282A=
XM_005267864.1:c.-278A= XP_005267921.1:n.-278A=
XM_005267866.1:c.-278A= XP_005267923.1:n.-278A=
XM_005267866.2:c.-278A= XP_005267923.1:n.-278A=