Canonical Allele Identifier: CA1725951656
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522157A= , CM000669.2:g.92522157A= GRCh38
NC_000007.13:g.92151471A= , CM000669.1:g.92151471A= GRCh37
NC_000007.12:g.91989407A= NCBI36
NG_008341.1:g.11375T=
NG_008341.2:g.11375T=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.218T= MANE Select ENSP00000248633.4:p.Val73=
ENST00000248633.8:c.218T= ENSP00000248633.4:p.Val73=
ENST00000428214.5:c.218T= ENSP00000394413.1:p.Val73=
ENST00000438045.5:c.218T= ENSP00000410438.1:p.Val73=
ENST00000484913.5:n.222T=
NM_000466.2:c.218T= NP_000457.1:p.Val73=
NM_001282677.1:c.218T= NP_001269606.1:p.Val73=
NM_001282678.1:c.-442T= NP_001269607.1:n.-442T=
XR_242246.3:n.314T=
XR_242246.5:n.265T=
NM_000466.3:c.218T= MANE Select NP_000457.1:p.Val73=
NM_001282677.2:c.218T= NP_001269606.1:p.Val73=
NM_001282678.2:c.-442T= NP_001269607.1:n.-442T=