Canonical Allele Identifier: CA368199325
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517651T>A , CM000669.2:g.92517651T>A GRCh38
NC_000007.13:g.92146965T>A , CM000669.1:g.92146965T>A GRCh37
NC_000007.12:g.91984901T>A NCBI36
NG_008341.1:g.15881A>T
NG_008341.2:g.15881A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.864A>T MANE Select ENSP00000248633.4:p.Arg288Ser
ENST00000248633.8:c.864A>T ENSP00000248633.4:p.Arg288Ser
ENST00000428214.5:c.864A>T ENSP00000394413.1:p.Arg288Ser
ENST00000438045.5:c.274-3684A>T ENSP00000410438.1:n.274-3684A>T
ENST00000484913.5:n.903A>T
NM_000466.2:c.864A>T NP_000457.1:p.Arg288Ser
NM_001282677.1:c.864A>T NP_001269606.1:p.Arg288Ser
NM_001282678.1:c.240A>T NP_001269607.1:p.Arg80Ser
XR_242246.3:n.960A>T
XR_242246.5:n.911A>T
NM_000466.3:c.864A>T MANE Select NP_000457.1:p.Arg288Ser
NM_001282677.2:c.864A>T NP_001269606.1:p.Arg288Ser
NM_001282678.2:c.240A>T NP_001269607.1:p.Arg80Ser