Canonical Allele Identifier: CA1725948255
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517992G= , CM000669.2:g.92517992G= GRCh38
NC_000007.13:g.92147306G= , CM000669.1:g.92147306G= GRCh37
NC_000007.12:g.91985242G= NCBI36
NG_008341.1:g.15540C=
NG_008341.2:g.15540C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.523C= MANE Select ENSP00000248633.4:p.Leu175=
ENST00000248633.8:c.523C= ENSP00000248633.4:p.Leu175=
ENST00000428214.5:c.523C= ENSP00000394413.1:p.Leu175=
ENST00000438045.5:c.274-4025C= ENSP00000410438.1:n.274-4025C=
ENST00000484913.5:n.562C=
NM_000466.2:c.523C= NP_000457.1:p.Leu175=
NM_001282677.1:c.523C= NP_001269606.1:p.Leu175=
NM_001282678.1:c.-102C= NP_001269607.1:n.-102C=
XR_242246.3:n.619C=
XR_242246.5:n.570C=
NM_000466.3:c.523C= MANE Select NP_000457.1:p.Leu175=
NM_001282677.2:c.523C= NP_001269606.1:p.Leu175=
NM_001282678.2:c.-102C= NP_001269607.1:n.-102C=