Canonical Allele Identifier: CA2776947501
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518360_92518362del , CM000669.2:g.92518360_92518362del GRCh38
NC_000007.13:g.92147674_92147676del , CM000669.1:g.92147674_92147676del GRCh37
NC_000007.12:g.91985610_91985612del NCBI36
NG_008341.1:g.15170_15172del
NG_008341.2:g.15170_15172del

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.358-107_358-105del MANE Select ENSP00000248633.4:n.358-107_358-105del
ENST00000248633.8:c.358-107_358-105del ENSP00000248633.4:n.358-107_358-105del
ENST00000428214.5:c.358-107_358-105del ENSP00000394413.1:n.358-107_358-105del
ENST00000438045.5:c.273+3740_273+3742del ENSP00000410438.1:n.273+3740_273+3742del
ENST00000484913.5:n.397-107_397-105del
NM_000466.2:c.358-107_358-105del NP_000457.1:n.358-107_358-105del
NM_001282677.1:c.358-107_358-105del NP_001269606.1:n.358-107_358-105del
NM_001282678.1:c.-267-107_-267-105del NP_001269607.1:n.-267-107_-267-105del
XR_242246.3:n.454-107_454-105del
XR_242246.5:n.405-107_405-105del
NM_000466.3:c.358-107_358-105del MANE Select NP_000457.1:n.358-107_358-105del
NM_001282677.2:c.358-107_358-105del NP_001269606.1:n.358-107_358-105del
NM_001282678.2:c.-267-107_-267-105del NP_001269607.1:n.-267-107_-267-105del