Canonical Allele Identifier: CA2776947510
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518397T>A , CM000669.2:g.92518397T>A GRCh38
NC_000007.13:g.92147711T>A , CM000669.1:g.92147711T>A GRCh37
NC_000007.12:g.91985647T>A NCBI36
NG_008341.1:g.15135A>T
NG_008341.2:g.15135A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.358-142A>T MANE Select ENSP00000248633.4:n.358-142A>T
ENST00000248633.8:c.358-142A>T ENSP00000248633.4:n.358-142A>T
ENST00000428214.5:c.358-142A>T ENSP00000394413.1:n.358-142A>T
ENST00000438045.5:c.273+3705A>T ENSP00000410438.1:n.273+3705A>T
ENST00000484913.5:n.397-142A>T
NM_000466.2:c.358-142A>T NP_000457.1:n.358-142A>T
NM_001282677.1:c.358-142A>T NP_001269606.1:n.358-142A>T
NM_001282678.1:c.-267-142A>T NP_001269607.1:n.-267-142A>T
XR_242246.3:n.454-142A>T
XR_242246.5:n.405-142A>T
NM_000466.3:c.358-142A>T MANE Select NP_000457.1:n.358-142A>T
NM_001282677.2:c.358-142A>T NP_001269606.1:n.358-142A>T
NM_001282678.2:c.-267-142A>T NP_001269607.1:n.-267-142A>T