Canonical Allele Identifier: CA2578938323
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92519103_92519106del , CM000669.2:g.92519103_92519106del GRCh38
NC_000007.13:g.92148417_92148420del , CM000669.1:g.92148417_92148420del GRCh37
NC_000007.12:g.91986353_91986356del NCBI36
NG_008341.1:g.14426_14429del
NG_008341.2:g.14426_14429del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.274-28_274-25del MANE Select ENSP00000248633.4:n.274-28_274-25del
ENST00000248633.8:c.274-28_274-25del ENSP00000248633.4:n.274-28_274-25del
ENST00000428214.5:c.274-28_274-25del ENSP00000394413.1:n.274-28_274-25del
ENST00000438045.5:c.273+2996_273+2999del ENSP00000410438.1:n.273+2996_273+2999del
ENST00000484913.5:n.278-28_278-25del
NM_000466.2:c.274-28_274-25del NP_000457.1:n.274-28_274-25del
NM_001282677.1:c.274-28_274-25del NP_001269606.1:n.274-28_274-25del
NM_001282678.1:c.-386-28_-386-25del NP_001269607.1:n.-386-28_-386-25del
XR_242246.3:n.370-28_370-25del
XR_242246.5:n.321-28_321-25del
NM_000466.3:c.274-28_274-25del MANE Select NP_000457.1:n.274-28_274-25del
NM_001282677.2:c.274-28_274-25del NP_001269606.1:n.274-28_274-25del
NM_001282678.2:c.-386-28_-386-25del NP_001269607.1:n.-386-28_-386-25del