Canonical Allele Identifier: CA2776947668
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522306_92522307del , CM000669.2:g.92522306_92522307del GRCh38
NC_000007.13:g.92151620_92151621del , CM000669.1:g.92151620_92151621del GRCh37
NC_000007.12:g.91989556_91989557del NCBI36
NG_008341.1:g.11225_11226del
NG_008341.2:g.11225_11226del

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.130-62_130-61del MANE Select ENSP00000248633.4:n.130-62_130-61del
ENST00000248633.8:c.130-62_130-61del ENSP00000248633.4:n.130-62_130-61del
ENST00000428214.5:c.130-62_130-61del ENSP00000394413.1:n.130-62_130-61del
ENST00000438045.5:c.130-62_130-61del ENSP00000410438.1:n.130-62_130-61del
ENST00000484913.5:n.134-62_134-61del
NM_000466.2:c.130-62_130-61del NP_000457.1:n.130-62_130-61del
NM_001282677.1:c.130-62_130-61del NP_001269606.1:n.130-62_130-61del
NM_001282678.1:c.-530-62_-530-61del NP_001269607.1:n.-530-62_-530-61del
XR_242246.3:n.226-62_226-61del
XR_242246.5:n.177-62_177-61del
NM_000466.3:c.130-62_130-61del MANE Select NP_000457.1:n.130-62_130-61del
NM_001282677.2:c.130-62_130-61del NP_001269606.1:n.130-62_130-61del
NM_001282678.2:c.-530-62_-530-61del NP_001269607.1:n.-530-62_-530-61del