Canonical Allele Identifier: CA2776947674
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522321_92522329del , CM000669.2:g.92522321_92522329del GRCh38
NC_000007.13:g.92151635_92151643del , CM000669.1:g.92151635_92151643del GRCh37
NC_000007.12:g.91989571_91989579del NCBI36
NG_008341.1:g.11203_11211del
NG_008341.2:g.11203_11211del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.130-84_130-76del MANE Select ENSP00000248633.4:n.130-84_130-76del
ENST00000248633.8:c.130-84_130-76del ENSP00000248633.4:n.130-84_130-76del
ENST00000428214.5:c.130-84_130-76del ENSP00000394413.1:n.130-84_130-76del
ENST00000438045.5:c.130-84_130-76del ENSP00000410438.1:n.130-84_130-76del
ENST00000484913.5:n.134-84_134-76del
NM_000466.2:c.130-84_130-76del NP_000457.1:n.130-84_130-76del
NM_001282677.1:c.130-84_130-76del NP_001269606.1:n.130-84_130-76del
NM_001282678.1:c.-530-84_-530-76del NP_001269607.1:n.-530-84_-530-76del
XR_242246.3:n.226-84_226-76del
XR_242246.5:n.177-84_177-76del
NM_000466.3:c.130-84_130-76del MANE Select NP_000457.1:n.130-84_130-76del
NM_001282677.2:c.130-84_130-76del NP_001269606.1:n.130-84_130-76del
NM_001282678.2:c.-530-84_-530-76del NP_001269607.1:n.-530-84_-530-76del