Canonical Allele Identifier: CA1725947198
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517357T= , CM000669.2:g.92517357T= GRCh38
NC_000007.13:g.92146671T= , CM000669.1:g.92146671T= GRCh37
NC_000007.12:g.91984607T= NCBI36
NG_008341.1:g.16175A=
NG_008341.2:g.16175A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.1158A= MANE Select ENSP00000248633.4:p.Val386=
ENST00000248633.8:c.1158A= ENSP00000248633.4:p.Val386=
ENST00000422866.1:c.59A=
ENST00000428214.5:c.1158A= ENSP00000394413.1:p.Val386=
ENST00000438045.5:c.274-3390A= ENSP00000410438.1:n.274-3390A=
ENST00000484913.5:n.1197A=
NM_000466.2:c.1158A= NP_000457.1:p.Val386=
NM_001282677.1:c.1158A= NP_001269606.1:p.Val386=
NM_001282678.1:c.534A= NP_001269607.1:p.Val178=
XR_242246.3:n.1254A=
XM_017012319.2:c.-509A= XP_016867808.1:n.-509A=
XR_001744808.2:n.268A=
XR_242246.5:n.1205A=
NM_000466.3:c.1158A= MANE Select NP_000457.1:p.Val386=
NM_001282677.2:c.1158A= NP_001269606.1:p.Val386=
NM_001282678.2:c.534A= NP_001269607.1:p.Val178=