Canonical Allele Identifier: CA1725948199
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517973G= , CM000669.2:g.92517973G= GRCh38
NC_000007.13:g.92147287G= , CM000669.1:g.92147287G= GRCh37
NC_000007.12:g.91985223G= NCBI36
NG_008341.1:g.15559C=
NG_008341.2:g.15559C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.542C= MANE Select ENSP00000248633.4:p.Thr181=
ENST00000248633.8:c.542C= ENSP00000248633.4:p.Thr181=
ENST00000428214.5:c.542C= ENSP00000394413.1:p.Thr181=
ENST00000438045.5:c.274-4006C= ENSP00000410438.1:n.274-4006C=
ENST00000484913.5:n.581C=
NM_000466.2:c.542C= NP_000457.1:p.Thr181=
NM_001282677.1:c.542C= NP_001269606.1:p.Thr181=
NM_001282678.1:c.-83C= NP_001269607.1:n.-83C=
XR_242246.3:n.638C=
XR_242246.5:n.589C=
NM_000466.3:c.542C= MANE Select NP_000457.1:p.Thr181=
NM_001282677.2:c.542C= NP_001269606.1:p.Thr181=
NM_001282678.2:c.-83C= NP_001269607.1:n.-83C=