Canonical Allele Identifier: CA390306097
Gene: PSEN1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.73219204C>T , CM000676.2:g.73219204C>T GRCh38
NC_000014.8:g.73685912C>T , CM000676.1:g.73685912C>T GRCh37
NC_000014.7:g.72755665C>T NCBI36
NG_007386.2:g.87734C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000324501.10:c.1319C>T MANE Select ENSP00000326366.5:p.Thr440Ile
ENST00000324501.9:c.1319C>T ENSP00000326366.5:p.Thr440Ile
ENST00000357710.8:c.1307C>T ENSP00000350342.4:p.Thr436Ile
ENST00000394164.5:c.1307C>T ENSP00000377719.1:p.Thr436Ile
ENST00000406768.1:c.1043C>T ENSP00000385948.1:p.Thr348Ile
ENST00000555386.5:n.1399C>T ENSP00000450845.1:n.1399C>T
ENST00000555867.1:n.684C>T
ENST00000557511.5:n.1145C>T ENSP00000451429.1:p.Thr382Ile
NM_000021.3:c.1319C>T NP_000012.1:p.Thr440Ile
NM_007318.2:c.1307C>T NP_015557.2:p.Thr436Ile
XM_005267864.1:c.1319C>T XP_005267921.1:p.Thr440Ile
XM_005267866.1:c.1307C>T XP_005267923.1:p.Thr436Ile
XM_011536971.1:c.1319C>T XP_011535273.1:p.Thr440Ile
XM_011536972.1:c.1319C>T XP_011535274.1:p.Thr440Ile
XM_011536973.1:c.1307C>T XP_011535275.1:p.Thr436Ile
XM_011536974.1:c.1307C>T XP_011535276.1:p.Thr436Ile
XM_005267864.3:c.1319C>T XP_005267921.1:p.Thr440Ile
XM_005267866.2:c.1307C>T XP_005267923.1:p.Thr436Ile
XM_011536972.2:c.1319C>T XP_011535274.1:p.Thr440Ile
XM_011536973.2:c.1307C>T XP_011535275.1:p.Thr436Ile
XM_011536974.2:c.1307C>T XP_011535276.1:p.Thr436Ile
NM_000021.4:c.1319C>T MANE Select NP_000012.1:p.Thr440Ile
NM_007318.3:c.1307C>T NP_015557.2:p.Thr436Ile