Canonical Allele Identifier: CA368204649
Community Standard Title: NM_000466.3(PEX1):c.273+1G>A
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522101C>T , CM000669.2:g.92522101C>T GRCh38
NC_000007.13:g.92151415C>T , CM000669.1:g.92151415C>T GRCh37
NC_000007.12:g.91989351C>T NCBI36
NG_008341.1:g.11431G>A
NG_008341.2:g.11431G>A

Transcript Alleles

HGVS Amino-acid Change
NM_000466.3:c.273+1G>A MANE Select NP_000457.1:n.273+1G>A
ENST00000248633.9:c.273+1G>A MANE Select ENSP00000248633.4:n.273+1G>A
NM_000466.2:c.273+1G>A NP_000457.1:n.273+1G>A
NM_001282677.1:c.273+1G>A NP_001269606.1:n.273+1G>A
NM_001282677.2:c.273+1G>A NP_001269606.1:n.273+1G>A
NM_001282678.1:c.-387+1G>A NP_001269607.1:n.-387+1G>A
NM_001282678.2:c.-387+1G>A NP_001269607.1:n.-387+1G>A
ENST00000248633.8:c.273+1G>A ENSP00000248633.4:n.273+1G>A
ENST00000428214.5:c.273+1G>A ENSP00000394413.1:n.273+1G>A
ENST00000438045.5:c.273+1G>A ENSP00000410438.1:n.273+1G>A
ENST00000484913.5:n.277+1G>A
XR_242246.3:n.369+1G>A
XR_242246.5:n.320+1G>A