Canonical Allele Identifier: CA1725951567
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92521983T= , CM000669.2:g.92521983T= GRCh38
NC_000007.13:g.92151297T= , CM000669.1:g.92151297T= GRCh37
NC_000007.12:g.91989233T= NCBI36
NG_008341.1:g.11549A=
NG_008341.2:g.11549A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.273+119A= MANE Select ENSP00000248633.4:n.273+119A=
ENST00000248633.8:c.273+119A= ENSP00000248633.4:n.273+119A=
ENST00000428214.5:c.273+119A= ENSP00000394413.1:n.273+119A=
ENST00000438045.5:c.273+119A= ENSP00000410438.1:n.273+119A=
ENST00000484913.5:n.277+119A=
NM_000466.2:c.273+119A= NP_000457.1:n.273+119A=
NM_001282677.1:c.273+119A= NP_001269606.1:n.273+119A=
NM_001282678.1:c.-387+119A= NP_001269607.1:n.-387+119A=
XR_242246.3:n.369+119A=
XR_242246.5:n.320+119A=
NM_000466.3:c.273+119A= MANE Select NP_000457.1:n.273+119A=
NM_001282677.2:c.273+119A= NP_001269606.1:n.273+119A=
NM_001282678.2:c.-387+119A= NP_001269607.1:n.-387+119A=