Canonical Allele Identifier: CA1725951676
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522212G= , CM000669.2:g.92522212G= GRCh38
NC_000007.13:g.92151526G= , CM000669.1:g.92151526G= GRCh37
NC_000007.12:g.91989462G= NCBI36
NG_008341.1:g.11320C=
NG_008341.2:g.11320C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.163C= MANE Select ENSP00000248633.4:p.Pro55=
ENST00000248633.8:c.163C= ENSP00000248633.4:p.Pro55=
ENST00000428214.5:c.163C= ENSP00000394413.1:p.Pro55=
ENST00000438045.5:c.163C= ENSP00000410438.1:p.Pro55=
ENST00000484913.5:n.167C=
NM_000466.2:c.163C= NP_000457.1:p.Pro55=
NM_001282677.1:c.163C= NP_001269606.1:p.Pro55=
NM_001282678.1:c.-497C= NP_001269607.1:n.-497C=
XR_242246.3:n.259C=
XR_242246.5:n.210C=
NM_000466.3:c.163C= MANE Select NP_000457.1:p.Pro55=
NM_001282677.2:c.163C= NP_001269606.1:p.Pro55=
NM_001282678.2:c.-497C= NP_001269607.1:n.-497C=