Canonical Allele Identifier: CA487097977

Gene: PSEN1

Linked Data

• MyVariant Identifiers: chr14:g.73640298T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.73173590T>C , CM000676.2:g.73173590T>C	GRCh38
NC_000014.8:g.73640298T>C , CM000676.1:g.73640298T>C	GRCh37
NC_000014.7:g.72710051T>C	NCBI36
NG_007386.2:g.42120T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000324501.10:c.363T>C MANE Select	ENSP00000326366.5:p.Asp121=
ENST00000324501.9:c.363T>C	ENSP00000326366.5:p.Asp121=
ENST00000357710.8:c.351T>C	ENSP00000350342.4:p.Asp117=
ENST00000394157.7:c.363T>C	ENSP00000377712.3:p.Asp121=
ENST00000394164.5:c.351T>C	ENSP00000377719.1:p.Asp117=
ENST00000406768.1:c.87T>C	ENSP00000385948.1:p.Asp29=
ENST00000553719.5:c.351T>C	ENSP00000451674.1:p.Asp117=
ENST00000553855.5:n.363T>C	ENSP00000452242.1:p.Asp121=
ENST00000555254.5:c.363T>C	ENSP00000450652.1:p.Asp121=
ENST00000555386.5:n.351T>C	ENSP00000450845.1:p.Asp117=
ENST00000557356.5:c.351T>C	ENSP00000451498.1:p.Asp117=
ENST00000557511.5:n.363T>C	ENSP00000451429.1:p.Asp121=
ENST00000559361.5:c.*307T>C	ENSP00000454156.1:n.*307T>C
NM_000021.3:c.363T>C	NP_000012.1:p.Asp121=
NM_007318.2:c.351T>C	NP_015557.2:p.Asp117=
XM_005267864.1:c.363T>C	XP_005267921.1:p.Asp121=
XM_005267866.1:c.351T>C	XP_005267923.1:p.Asp117=
XM_011536971.1:c.363T>C	XP_011535273.1:p.Asp121=
XM_011536972.1:c.363T>C	XP_011535274.1:p.Asp121=
XM_011536973.1:c.351T>C	XP_011535275.1:p.Asp117=
XM_011536974.1:c.351T>C	XP_011535276.1:p.Asp117=
XM_005267864.3:c.363T>C	XP_005267921.1:p.Asp121=
XM_005267866.2:c.351T>C	XP_005267923.1:p.Asp117=
XM_011536972.2:c.363T>C	XP_011535274.1:p.Asp121=
XM_011536973.2:c.351T>C	XP_011535275.1:p.Asp117=
XM_011536974.2:c.351T>C	XP_011535276.1:p.Asp117=
NM_000021.4:c.363T>C MANE Select	NP_000012.1:p.Asp121=
NM_007318.3:c.351T>C	NP_015557.2:p.Asp117=