Canonical Allele Identifier: CA1725949144
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518867G= , CM000669.2:g.92518867G= GRCh38
NC_000007.13:g.92148181G= , CM000669.1:g.92148181G= GRCh37
NC_000007.12:g.91986117G= NCBI36
NG_008341.1:g.14665C=
NG_008341.2:g.14665C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.357+128C= MANE Select ENSP00000248633.4:n.357+128C=
ENST00000248633.8:c.357+128C= ENSP00000248633.4:n.357+128C=
ENST00000428214.5:c.357+128C= ENSP00000394413.1:n.357+128C=
ENST00000438045.5:c.273+3235C= ENSP00000410438.1:n.273+3235C=
ENST00000484913.5:n.396+93C=
NM_000466.2:c.357+128C= NP_000457.1:n.357+128C=
NM_001282677.1:c.357+128C= NP_001269606.1:n.357+128C=
NM_001282678.1:c.-268+93C= NP_001269607.1:n.-268+93C=
XR_242246.3:n.453+128C=
XR_242246.5:n.404+128C=
NM_000466.3:c.357+128C= MANE Select NP_000457.1:n.357+128C=
NM_001282677.2:c.357+128C= NP_001269606.1:n.357+128C=
NM_001282678.2:c.-268+93C= NP_001269607.1:n.-268+93C=