Canonical Allele Identifier: CA2776947679
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522329_92522341del , CM000669.2:g.92522329_92522341del GRCh38
NC_000007.13:g.92151643_92151655del , CM000669.1:g.92151643_92151655del GRCh37
NC_000007.12:g.91989579_91989591del NCBI36
NG_008341.1:g.11191_11203del
NG_008341.2:g.11191_11203del

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.130-96_130-84del MANE Select ENSP00000248633.4:n.130-96_130-84del
ENST00000248633.8:c.130-96_130-84del ENSP00000248633.4:n.130-96_130-84del
ENST00000428214.5:c.130-96_130-84del ENSP00000394413.1:n.130-96_130-84del
ENST00000438045.5:c.130-96_130-84del ENSP00000410438.1:n.130-96_130-84del
ENST00000484913.5:n.134-96_134-84del
NM_000466.2:c.130-96_130-84del NP_000457.1:n.130-96_130-84del
NM_001282677.1:c.130-96_130-84del NP_001269606.1:n.130-96_130-84del
NM_001282678.1:c.-530-96_-530-84del NP_001269607.1:n.-530-96_-530-84del
XR_242246.3:n.226-96_226-84del
XR_242246.5:n.177-96_177-84del
NM_000466.3:c.130-96_130-84del MANE Select NP_000457.1:n.130-96_130-84del
NM_001282677.2:c.130-96_130-84del NP_001269606.1:n.130-96_130-84del
NM_001282678.2:c.-530-96_-530-84del NP_001269607.1:n.-530-96_-530-84del