Canonical Allele Identifier: CA1725948459
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518156T= , CM000669.2:g.92518156T= GRCh38
NC_000007.13:g.92147470T= , CM000669.1:g.92147470T= GRCh37
NC_000007.12:g.91985406T= NCBI36
NG_008341.1:g.15376A=
NG_008341.2:g.15376A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.457A= MANE Select ENSP00000248633.4:p.Ile153=
ENST00000248633.8:c.457A= ENSP00000248633.4:p.Ile153=
ENST00000428214.5:c.457A= ENSP00000394413.1:p.Ile153=
ENST00000438045.5:c.273+3946A= ENSP00000410438.1:n.273+3946A=
ENST00000484913.5:n.496A=
NM_000466.2:c.457A= NP_000457.1:p.Ile153=
NM_001282677.1:c.457A= NP_001269606.1:p.Ile153=
NM_001282678.1:c.-168A= NP_001269607.1:n.-168A=
XR_242246.3:n.553A=
XR_242246.5:n.504A=
NM_000466.3:c.457A= MANE Select NP_000457.1:p.Ile153=
NM_001282677.2:c.457A= NP_001269606.1:p.Ile153=
NM_001282678.2:c.-168A= NP_001269607.1:n.-168A=