Canonical Allele Identifier: CA2695207996
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522105del , CM000669.2:g.92522105del GRCh38
NC_000007.13:g.92151419del , CM000669.1:g.92151419del GRCh37
NC_000007.12:g.91989355del NCBI36
NG_008341.1:g.11427del
NG_008341.2:g.11427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.270del MANE Select ENSP00000248633.4:p.Gln91ArgfsTer?
ENST00000248633.8:c.270del ENSP00000248633.4:p.Gln91ArgfsTer?
ENST00000428214.5:c.270del ENSP00000394413.1:p.Gln91ArgfsTer?
ENST00000438045.5:c.270del ENSP00000410438.1:p.Gln91ArgfsTer6
ENST00000484913.5:n.274del
NM_000466.2:c.270del NP_000457.1:p.Gln91ArgfsTer?
NM_001282677.1:c.270del NP_001269606.1:p.Gln91ArgfsTer?
NM_001282678.1:c.-390del NP_001269607.1:n.-390del
XR_242246.3:n.366del
XR_242246.5:n.317del
NM_000466.3:c.270del MANE Select NP_000457.1:p.Gln91ArgfsTer?
NM_001282677.2:c.270del NP_001269606.1:p.Gln91ArgfsTer?
NM_001282678.2:c.-390del NP_001269607.1:n.-390del