Canonical Allele Identifier: CA2776946095
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92499946del , CM000669.2:g.92499946del GRCh38
NC_000007.13:g.92129260del , CM000669.1:g.92129260del GRCh37
NC_000007.12:g.91967196del NCBI36
NG_008341.1:g.33586del
NG_008341.2:g.33586del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2584-108del MANE Select ENSP00000248633.4:n.2584-108del
ENST00000248633.8:c.2584-108del ENSP00000248633.4:n.2584-108del
ENST00000428214.5:c.2413-108del ENSP00000394413.1:n.2413-108del
ENST00000438045.5:c.1618-108del ENSP00000410438.1:n.1618-108del
ENST00000484913.5:n.2623-108del
ENST00000496420.5:n.2476-108del
NM_000466.2:c.2584-108del NP_000457.1:n.2584-108del
NM_001282677.1:c.2413-108del NP_001269606.1:n.2413-108del
NM_001282678.1:c.1960-108del NP_001269607.1:n.1960-108del
XM_005250433.3:c.835-108del XP_005250490.1:n.835-108del
XR_242246.3:n.2680-108del
XM_017012319.2:c.835-108del XP_016867808.1:n.835-108del
XR_001744808.2:n.1611-108del
XR_242246.5:n.2631-108del
NM_000466.3:c.2584-108del MANE Select NP_000457.1:n.2584-108del
NM_001282677.2:c.2413-108del NP_001269606.1:n.2413-108del
NM_001282678.2:c.1960-108del NP_001269607.1:n.1960-108del