Canonical Allele Identifier: CA2776947453
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518317_92518331del , CM000669.2:g.92518317_92518331del GRCh38
NC_000007.13:g.92147631_92147645del , CM000669.1:g.92147631_92147645del GRCh37
NC_000007.12:g.91985567_91985581del NCBI36
NG_008341.1:g.15201_15215del
NG_008341.2:g.15201_15215del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.358-76_358-62del MANE Select ENSP00000248633.4:n.358-76_358-62del
ENST00000248633.8:c.358-76_358-62del ENSP00000248633.4:n.358-76_358-62del
ENST00000428214.5:c.358-76_358-62del ENSP00000394413.1:n.358-76_358-62del
ENST00000438045.5:c.273+3771_273+3785del ENSP00000410438.1:n.273+3771_273+3785del
ENST00000484913.5:n.397-76_397-62del
NM_000466.2:c.358-76_358-62del NP_000457.1:n.358-76_358-62del
NM_001282677.1:c.358-76_358-62del NP_001269606.1:n.358-76_358-62del
NM_001282678.1:c.-267-76_-267-62del NP_001269607.1:n.-267-76_-267-62del
XR_242246.3:n.454-76_454-62del
XR_242246.5:n.405-76_405-62del
NM_000466.3:c.358-76_358-62del MANE Select NP_000457.1:n.358-76_358-62del
NM_001282677.2:c.358-76_358-62del NP_001269606.1:n.358-76_358-62del
NM_001282678.2:c.-267-76_-267-62del NP_001269607.1:n.-267-76_-267-62del