Canonical Allele Identifier: CA2776946316
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92502174_92502178del , CM000669.2:g.92502174_92502178del GRCh38
NC_000007.13:g.92131488_92131492del , CM000669.1:g.92131488_92131492del GRCh37
NC_000007.12:g.91969424_91969428del NCBI36
NG_008341.1:g.31354_31358del
NG_008341.2:g.31354_31358del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2227-99_2227-95del MANE Select ENSP00000248633.4:n.2227-99_2227-95del
ENST00000248633.8:c.2227-99_2227-95del ENSP00000248633.4:n.2227-99_2227-95del
ENST00000428214.5:c.2056-99_2056-95del ENSP00000394413.1:n.2056-99_2056-95del
ENST00000438045.5:c.1261-99_1261-95del ENSP00000410438.1:n.1261-99_1261-95del
ENST00000484913.5:n.2266-99_2266-95del
ENST00000496092.1:n.25-99_25-95del
ENST00000496420.5:n.1903-99_1903-95del
NM_000466.2:c.2227-99_2227-95del NP_000457.1:n.2227-99_2227-95del
NM_001282677.1:c.2056-99_2056-95del NP_001269606.1:n.2056-99_2056-95del
NM_001282678.1:c.1603-99_1603-95del NP_001269607.1:n.1603-99_1603-95del
XM_005250433.3:c.478-99_478-95del XP_005250490.1:n.478-99_478-95del
XR_242246.3:n.2323-99_2323-95del
XM_017012319.2:c.478-99_478-95del XP_016867808.1:n.478-99_478-95del
XR_001744808.2:n.1254-99_1254-95del
XR_242246.5:n.2274-99_2274-95del
NM_000466.3:c.2227-99_2227-95del MANE Select NP_000457.1:n.2227-99_2227-95del
NM_001282677.2:c.2056-99_2056-95del NP_001269606.1:n.2056-99_2056-95del
NM_001282678.2:c.1603-99_1603-95del NP_001269607.1:n.1603-99_1603-95del