Canonical Allele Identifier: CA1725947707
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517680T= , CM000669.2:g.92517680T= GRCh38
NC_000007.13:g.92146994T= , CM000669.1:g.92146994T= GRCh37
NC_000007.12:g.91984930T= NCBI36
NG_008341.1:g.15852A=
NG_008341.2:g.15852A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.835A= MANE Select ENSP00000248633.4:p.Lys279=
ENST00000248633.8:c.835A= ENSP00000248633.4:p.Lys279=
ENST00000428214.5:c.835A= ENSP00000394413.1:p.Lys279=
ENST00000438045.5:c.274-3713A= ENSP00000410438.1:n.274-3713A=
ENST00000484913.5:n.874A=
NM_000466.2:c.835A= NP_000457.1:p.Lys279=
NM_001282677.1:c.835A= NP_001269606.1:p.Lys279=
NM_001282678.1:c.211A= NP_001269607.1:p.Lys71=
XR_242246.3:n.931A=
XR_242246.5:n.882A=
NM_000466.3:c.835A= MANE Select NP_000457.1:p.Lys279=
NM_001282677.2:c.835A= NP_001269606.1:p.Lys279=
NM_001282678.2:c.211A= NP_001269607.1:p.Lys71=