Canonical Allele Identifier: CA262598415

Gene: PSEN1

Linked Data

• dbSNP Id: rs202022163
• gnomAD v3: 14-73136453-G-A
• gnomAD v4: 14-73136453-G-A
• MyVariant Identifiers: chr14:g.73603161G>A (hg19) ; chr14:g.73136453G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73136453G>A , CM000676.2:g.73136453G>A	GRCh38
NC_000014.8:g.73603161G>A , CM000676.1:g.73603161G>A	GRCh37
NC_000014.7:g.72672914G>A	NCBI36
NG_007386.2:g.4983G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000553599.6:c.-308G>A	ENSP00000452477.2:n.-308G>A
ENST00000555386.6:c.-266G>A	ENSP00000450845.1:n.-266G>A
ENST00000556011.6:c.-308G>A	ENSP00000451662.2:n.-308G>A
ENST00000556951.6:c.-262G>A	ENSP00000450551.2:n.-262G>A
ENST00000557293.6:c.-262G>A	ENSP00000451880.2:n.-262G>A
ENST00000697912.1:c.-266G>A	ENSP00000513477.1:n.-266G>A
ENST00000700265.1:c.-104+5G>A	ENSP00000514901.1:n.-104+5G>A
ENST00000700266.1:c.-266G>A	ENSP00000514902.1:n.-266G>A
ENST00000700267.1:c.-136+5G>A	ENSP00000514903.1:n.-136+5G>A
ENST00000700268.1:c.-262G>A	ENSP00000514904.1:n.-262G>A
ENST00000700269.1:c.-308G>A	ENSP00000514905.1:n.-308G>A
ENST00000700270.1:n.3G>A
ENST00000700271.1:c.-266G>A	ENSP00000514906.1:n.-266G>A
ENST00000700272.1:c.-262G>A	ENSP00000514907.1:n.-262G>A
ENST00000700273.1:c.-308G>A	ENSP00000514908.1:n.-308G>A
ENST00000700302.1:c.-266G>A	ENSP00000514929.1:n.-266G>A
ENST00000700303.1:c.-266G>A	ENSP00000514930.1:n.-266G>A
ENST00000324501.9:c.-266G>A	ENSP00000326366.5:n.-266G>A
ENST00000357710.8:c.-266G>A	ENSP00000350342.4:n.-266G>A
ENST00000394157.7:c.-266G>A	ENSP00000377712.3:n.-266G>A
ENST00000553599.5:c.-308G>A	ENSP00000452477.1:n.-308G>A
ENST00000553719.5:c.-262G>A	ENSP00000451674.1:n.-262G>A
ENST00000556011.5:c.-308G>A	ENSP00000451662.1:n.-308G>A
ENST00000556533.5:c.-255G>A	ENSP00000452128.1:n.-255G>A
ENST00000556864.5:c.-365G>A	ENSP00000451588.1:n.-365G>A
ENST00000556951.5:c.-262G>A	ENSP00000450551.1:n.-262G>A
ENST00000557293.5:c.-262G>A	ENSP00000451880.1:n.-262G>A
ENST00000557356.5:c.-136+5G>A	ENSP00000451498.1:n.-136+5G>A
ENST00000560005.6:c.-368G>A	ENSP00000453466.1:n.-368G>A
NM_000021.3:c.-266G>A	NP_000012.1:n.-266G>A
NM_007318.2:c.-266G>A	NP_015557.2:n.-266G>A
XM_005267864.1:c.-262G>A	XP_005267921.1:n.-262G>A
XM_005267866.1:c.-262G>A	XP_005267923.1:n.-262G>A
XM_005267864.3:c.-262G>A	XP_005267921.1:n.-262G>A
XM_005267866.2:c.-262G>A	XP_005267923.1:n.-262G>A