Canonical Allele Identifier: CA1725947793
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517725A= , CM000669.2:g.92517725A= GRCh38
NC_000007.13:g.92147039A= , CM000669.1:g.92147039A= GRCh37
NC_000007.12:g.91984975A= NCBI36
NG_008341.1:g.15807T=
NG_008341.2:g.15807T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.790T= MANE Select ENSP00000248633.4:p.Ser264=
ENST00000248633.8:c.790T= ENSP00000248633.4:p.Ser264=
ENST00000428214.5:c.790T= ENSP00000394413.1:p.Ser264=
ENST00000438045.5:c.274-3758T= ENSP00000410438.1:n.274-3758T=
ENST00000484913.5:n.829T=
NM_000466.2:c.790T= NP_000457.1:p.Ser264=
NM_001282677.1:c.790T= NP_001269606.1:p.Ser264=
NM_001282678.1:c.166T= NP_001269607.1:p.Ser56=
XR_242246.3:n.886T=
XR_242246.5:n.837T=
NM_000466.3:c.790T= MANE Select NP_000457.1:p.Ser264=
NM_001282677.2:c.790T= NP_001269606.1:p.Ser264=
NM_001282678.2:c.166T= NP_001269607.1:p.Ser56=