Canonical Allele Identifier: CA1725949386
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92519083A= , CM000669.2:g.92519083A= GRCh38
NC_000007.13:g.92148397A= , CM000669.1:g.92148397A= GRCh37
NC_000007.12:g.91986333A= NCBI36
NG_008341.1:g.14449T=
NG_008341.2:g.14449T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.274-5T= MANE Select ENSP00000248633.4:n.274-5T=
ENST00000248633.8:c.274-5T= ENSP00000248633.4:n.274-5T=
ENST00000428214.5:c.274-5T= ENSP00000394413.1:n.274-5T=
ENST00000438045.5:c.273+3019T= ENSP00000410438.1:n.273+3019T=
ENST00000484913.5:n.278-5T=
NM_000466.2:c.274-5T= NP_000457.1:n.274-5T=
NM_001282677.1:c.274-5T= NP_001269606.1:n.274-5T=
NM_001282678.1:c.-386-5T= NP_001269607.1:n.-386-5T=
XR_242246.3:n.370-5T=
XR_242246.5:n.321-5T=
NM_000466.3:c.274-5T= MANE Select NP_000457.1:n.274-5T=
NM_001282677.2:c.274-5T= NP_001269606.1:n.274-5T=
NM_001282678.2:c.-386-5T= NP_001269607.1:n.-386-5T=