Canonical Allele Identifier: CA1725948274
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518015C= , CM000669.2:g.92518015C= GRCh38
NC_000007.13:g.92147329C= , CM000669.1:g.92147329C= GRCh37
NC_000007.12:g.91985265C= NCBI36
NG_008341.1:g.15517G=
NG_008341.2:g.15517G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.500G= MANE Select ENSP00000248633.4:p.Gly167=
ENST00000248633.8:c.500G= ENSP00000248633.4:p.Gly167=
ENST00000428214.5:c.500G= ENSP00000394413.1:p.Gly167=
ENST00000438045.5:c.274-4048G= ENSP00000410438.1:n.274-4048G=
ENST00000484913.5:n.539G=
NM_000466.2:c.500G= NP_000457.1:p.Gly167=
NM_001282677.1:c.500G= NP_001269606.1:p.Gly167=
NM_001282678.1:c.-125G= NP_001269607.1:n.-125G=
XR_242246.3:n.596G=
XR_242246.5:n.547G=
NM_000466.3:c.500G= MANE Select NP_000457.1:p.Gly167=
NM_001282677.2:c.500G= NP_001269606.1:p.Gly167=
NM_001282678.2:c.-125G= NP_001269607.1:n.-125G=