Canonical Allele Identifier: CA2557048820
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518902G>A , CM000669.2:g.92518902G>A GRCh38
NC_000007.13:g.92148216G>A , CM000669.1:g.92148216G>A GRCh37
NC_000007.12:g.91986152G>A NCBI36
NG_008341.1:g.14630C>T
NG_008341.2:g.14630C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.357+93C>T MANE Select ENSP00000248633.4:n.357+93C>T
ENST00000248633.8:c.357+93C>T ENSP00000248633.4:n.357+93C>T
ENST00000428214.5:c.357+93C>T ENSP00000394413.1:n.357+93C>T
ENST00000438045.5:c.273+3200C>T ENSP00000410438.1:n.273+3200C>T
ENST00000484913.5:n.396+58C>T
NM_000466.2:c.357+93C>T NP_000457.1:n.357+93C>T
NM_001282677.1:c.357+93C>T NP_001269606.1:n.357+93C>T
NM_001282678.1:c.-268+58C>T NP_001269607.1:n.-268+58C>T
XR_242246.3:n.453+93C>T
XR_242246.5:n.404+93C>T
NM_000466.3:c.357+93C>T MANE Select NP_000457.1:n.357+93C>T
NM_001282677.2:c.357+93C>T NP_001269606.1:n.357+93C>T
NM_001282678.2:c.-268+58C>T NP_001269607.1:n.-268+58C>T