Canonical Allele Identifier: CA2683721231
Gene: PEX1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92521988_92521995del , CM000669.2:g.92521988_92521995del GRCh38
NC_000007.13:g.92151302_92151309del , CM000669.1:g.92151302_92151309del GRCh37
NC_000007.12:g.91989238_91989245del NCBI36
NG_008341.1:g.11537_11544del
NG_008341.2:g.11537_11544del

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.273+107_273+114del MANE Select ENSP00000248633.4:n.273+107_273+114del
ENST00000248633.8:c.273+107_273+114del ENSP00000248633.4:n.273+107_273+114del
ENST00000428214.5:c.273+107_273+114del ENSP00000394413.1:n.273+107_273+114del
ENST00000438045.5:c.273+107_273+114del ENSP00000410438.1:n.273+107_273+114del
ENST00000484913.5:n.277+107_277+114del
NM_000466.2:c.273+107_273+114del NP_000457.1:n.273+107_273+114del
NM_001282677.1:c.273+107_273+114del NP_001269606.1:n.273+107_273+114del
NM_001282678.1:c.-387+107_-387+114del NP_001269607.1:n.-387+107_-387+114del
XR_242246.3:n.369+107_369+114del
XR_242246.5:n.320+107_320+114del
NM_000466.3:c.273+107_273+114del MANE Select NP_000457.1:n.273+107_273+114del
NM_001282677.2:c.273+107_273+114del NP_001269606.1:n.273+107_273+114del
NM_001282678.2:c.-387+107_-387+114del NP_001269607.1:n.-387+107_-387+114del