Canonical Allele Identifier: CA2146453835
Gene: PSEN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73136440A= , CM000676.2:g.73136440A= GRCh38
NC_000014.8:g.73603148A= , CM000676.1:g.73603148A= GRCh37
NC_000014.7:g.72672901A= NCBI36
NG_007386.2:g.4970A=

Transcript Alleles

HGVS Amino-acid change
ENST00000556951.6:c.-275A= ENSP00000450551.2:n.-275A=
ENST00000557293.6:c.-275A= ENSP00000451880.2:n.-275A=
ENST00000700265.1:c.-112A= ENSP00000514901.1:n.-112A=
ENST00000700266.1:c.-279A= ENSP00000514902.1:n.-279A=
ENST00000700267.1:c.-144A= ENSP00000514903.1:n.-144A=
ENST00000700268.1:c.-275A= ENSP00000514904.1:n.-275A=
ENST00000556533.5:c.-268A= ENSP00000452128.1:n.-268A=
ENST00000556864.5:c.-378A= ENSP00000451588.1:n.-378A=
ENST00000556951.5:c.-275A= ENSP00000450551.1:n.-275A=
ENST00000557293.5:c.-275A= ENSP00000451880.1:n.-275A=
ENST00000557356.5:c.-144A= ENSP00000451498.1:n.-144A=
NM_000021.3:c.-279A= NP_000012.1:n.-279A=
NM_007318.2:c.-279A= NP_015557.2:n.-279A=
XM_005267864.1:c.-275A= XP_005267921.1:n.-275A=
XM_005267866.1:c.-275A= XP_005267923.1:n.-275A=
XM_005267866.2:c.-275A= XP_005267923.1:n.-275A=