Canonical Allele Identifier: CA1725947650
Gene: PEX1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.864A= MANE Select ENSP00000248633.4:p.Arg288=
ENST00000248633.8:c.864A= ENSP00000248633.4:p.Arg288=
ENST00000428214.5:c.864A= ENSP00000394413.1:p.Arg288=
ENST00000438045.5:c.274-3684A= ENSP00000410438.1:n.274-3684A=
ENST00000484913.5:n.903A=
NM_000466.2:c.864A= NP_000457.1:p.Arg288=
NM_001282677.1:c.864A= NP_001269606.1:p.Arg288=
NM_001282678.1:c.240A= NP_001269607.1:p.Arg80=
XR_242246.3:n.960A=
XR_242246.5:n.911A=
NM_000466.3:c.864A= MANE Select NP_000457.1:p.Arg288=
NM_001282677.2:c.864A= NP_001269606.1:p.Arg288=
NM_001282678.2:c.240A= NP_001269607.1:p.Arg80=