Canonical Allele Identifier: CA1725949241
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518973G= , CM000669.2:g.92518973G= GRCh38
NC_000007.13:g.92148287G= , CM000669.1:g.92148287G= GRCh37
NC_000007.12:g.91986223G= NCBI36
NG_008341.1:g.14559C=
NG_008341.2:g.14559C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.357+22C= MANE Select ENSP00000248633.4:n.357+22C=
ENST00000248633.8:c.357+22C= ENSP00000248633.4:n.357+22C=
ENST00000428214.5:c.357+22C= ENSP00000394413.1:n.357+22C=
ENST00000438045.5:c.273+3129C= ENSP00000410438.1:n.273+3129C=
ENST00000484913.5:n.383C=
NM_000466.2:c.357+22C= NP_000457.1:n.357+22C=
NM_001282677.1:c.357+22C= NP_001269606.1:n.357+22C=
NM_001282678.1:c.-281C= NP_001269607.1:n.-281C=
XR_242246.3:n.453+22C=
XR_242246.5:n.404+22C=
NM_000466.3:c.357+22C= MANE Select NP_000457.1:n.357+22C=
NM_001282677.2:c.357+22C= NP_001269606.1:n.357+22C=
NM_001282678.2:c.-281C= NP_001269607.1:n.-281C=