Canonical Allele Identifier: CA1725949343
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92519049T= , CM000669.2:g.92519049T= GRCh38
NC_000007.13:g.92148363T= , CM000669.1:g.92148363T= GRCh37
NC_000007.12:g.91986299T= NCBI36
NG_008341.1:g.14483A=
NG_008341.2:g.14483A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.303A= MANE Select ENSP00000248633.4:p.Val101=
ENST00000248633.8:c.303A= ENSP00000248633.4:p.Val101=
ENST00000428214.5:c.303A= ENSP00000394413.1:p.Val101=
ENST00000438045.5:c.273+3053A= ENSP00000410438.1:n.273+3053A=
ENST00000484913.5:n.307A=
NM_000466.2:c.303A= NP_000457.1:p.Val101=
NM_001282677.1:c.303A= NP_001269606.1:p.Val101=
NM_001282678.1:c.-357A= NP_001269607.1:n.-357A=
XR_242246.3:n.399A=
XR_242246.5:n.350A=
NM_000466.3:c.303A= MANE Select NP_000457.1:p.Val101=
NM_001282677.2:c.303A= NP_001269606.1:p.Val101=
NM_001282678.2:c.-357A= NP_001269607.1:n.-357A=