Canonical Allele Identifier: CA1725948680
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518315T= , CM000669.2:g.92518315T= GRCh38
NC_000007.13:g.92147629T= , CM000669.1:g.92147629T= GRCh37
NC_000007.12:g.91985565T= NCBI36
NG_008341.1:g.15217A=
NG_008341.2:g.15217A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.358-60A= MANE Select ENSP00000248633.4:n.358-60A=
ENST00000248633.8:c.358-60A= ENSP00000248633.4:n.358-60A=
ENST00000428214.5:c.358-60A= ENSP00000394413.1:n.358-60A=
ENST00000438045.5:c.273+3787A= ENSP00000410438.1:n.273+3787A=
ENST00000484913.5:n.397-60A=
NM_000466.2:c.358-60A= NP_000457.1:n.358-60A=
NM_001282677.1:c.358-60A= NP_001269606.1:n.358-60A=
NM_001282678.1:c.-267-60A= NP_001269607.1:n.-267-60A=
XR_242246.3:n.454-60A=
XR_242246.5:n.405-60A=
NM_000466.3:c.358-60A= MANE Select NP_000457.1:n.358-60A=
NM_001282677.2:c.358-60A= NP_001269606.1:n.358-60A=
NM_001282678.2:c.-267-60A= NP_001269607.1:n.-267-60A=