Canonical Allele Identifier: CA487255438

Gene: PSEN1

Linked Data

• MyVariant Identifiers: chr14:g.73637540A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73170832A>G , CM000676.2:g.73170832A>G	GRCh38
NC_000014.8:g.73637540A>G , CM000676.1:g.73637540A>G	GRCh37
NC_000014.7:g.72707293A>G	NCBI36
NG_007386.2:g.39362A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000324501.10:c.123A>G MANE Select	ENSP00000326366.5:p.Arg41=
ENST00000324501.9:c.123A>G	ENSP00000326366.5:p.Arg41=
ENST00000357710.8:c.111A>G	ENSP00000350342.4:p.Arg37=
ENST00000394157.7:c.123A>G	ENSP00000377712.3:p.Arg41=
ENST00000394164.5:c.111A>G	ENSP00000377719.1:p.Arg37=
ENST00000406768.1:c.-154A>G	ENSP00000385948.1:n.-154A>G
ENST00000553447.6:n.520A>G
ENST00000553599.5:c.111A>G	ENSP00000452477.1:p.Arg37=
ENST00000553719.5:c.111A>G	ENSP00000451674.1:p.Arg37=
ENST00000553855.5:n.123A>G	ENSP00000452242.1:p.Arg41=
ENST00000554131.5:c.123A>G	ENSP00000451915.1:p.Arg41=
ENST00000555254.5:c.123A>G	ENSP00000450652.1:p.Arg41=
ENST00000555386.5:n.111A>G	ENSP00000450845.1:p.Arg37=
ENST00000556066.1:c.111A>G	ENSP00000452267.1:p.Arg37=
ENST00000556533.5:c.111A>G	ENSP00000452128.1:p.Arg37=
ENST00000556864.5:c.111A>G	ENSP00000451588.1:p.Arg37=
ENST00000556951.5:c.111A>G	ENSP00000450551.1:p.Arg37=
ENST00000557037.5:c.111A>G	ENSP00000451347.1:p.Arg37=
ENST00000557293.5:c.123A>G	ENSP00000451880.1:p.Arg41=
ENST00000557356.5:c.111A>G	ENSP00000451498.1:p.Arg37=
ENST00000557511.5:n.123A>G	ENSP00000451429.1:p.Arg41=
ENST00000559361.5:c.*67A>G	ENSP00000454156.1:n.*67A>G
ENST00000560005.6:c.111A>G	ENSP00000453466.1:p.Arg37=
NM_000021.3:c.123A>G	NP_000012.1:p.Arg41=
NM_007318.2:c.111A>G	NP_015557.2:p.Arg37=
XM_005267864.1:c.123A>G	XP_005267921.1:p.Arg41=
XM_005267866.1:c.111A>G	XP_005267923.1:p.Arg37=
XM_011536971.1:c.123A>G	XP_011535273.1:p.Arg41=
XM_011536972.1:c.123A>G	XP_011535274.1:p.Arg41=
XM_011536973.1:c.111A>G	XP_011535275.1:p.Arg37=
XM_011536974.1:c.111A>G	XP_011535276.1:p.Arg37=
XM_005267864.3:c.123A>G	XP_005267921.1:p.Arg41=
XM_005267866.2:c.111A>G	XP_005267923.1:p.Arg37=
XM_011536972.2:c.123A>G	XP_011535274.1:p.Arg41=
XM_011536973.2:c.111A>G	XP_011535275.1:p.Arg37=
XM_011536974.2:c.111A>G	XP_011535276.1:p.Arg37=
NM_000021.4:c.123A>G MANE Select	NP_000012.1:p.Arg41=
NM_007318.3:c.111A>G	NP_015557.2:p.Arg37=