Canonical Allele Identifier: CA1725948530
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518209C= , CM000669.2:g.92518209C= GRCh38
NC_000007.13:g.92147523C= , CM000669.1:g.92147523C= GRCh37
NC_000007.12:g.91985459C= NCBI36
NG_008341.1:g.15323G=
NG_008341.2:g.15323G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.404G= MANE Select ENSP00000248633.4:p.Arg135=
ENST00000248633.8:c.404G= ENSP00000248633.4:p.Arg135=
ENST00000428214.5:c.404G= ENSP00000394413.1:p.Arg135=
ENST00000438045.5:c.273+3893G= ENSP00000410438.1:n.273+3893G=
ENST00000484913.5:n.443G=
NM_000466.2:c.404G= NP_000457.1:p.Arg135=
NM_001282677.1:c.404G= NP_001269606.1:p.Arg135=
NM_001282678.1:c.-221G= NP_001269607.1:n.-221G=
XR_242246.3:n.500G=
XR_242246.5:n.451G=
NM_000466.3:c.404G= MANE Select NP_000457.1:p.Arg135=
NM_001282677.2:c.404G= NP_001269606.1:p.Arg135=
NM_001282678.2:c.-221G= NP_001269607.1:n.-221G=