Canonical Allele Identifier: CA1725947581
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517614A= , CM000669.2:g.92517614A= GRCh38
NC_000007.13:g.92146928A= , CM000669.1:g.92146928A= GRCh37
NC_000007.12:g.91984864A= NCBI36
NG_008341.1:g.15918T=
NG_008341.2:g.15918T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.901T= MANE Select ENSP00000248633.4:p.Ser301=
ENST00000248633.8:c.901T= ENSP00000248633.4:p.Ser301=
ENST00000428214.5:c.901T= ENSP00000394413.1:p.Ser301=
ENST00000438045.5:c.274-3647T= ENSP00000410438.1:n.274-3647T=
ENST00000484913.5:n.940T=
NM_000466.2:c.901T= NP_000457.1:p.Ser301=
NM_001282677.1:c.901T= NP_001269606.1:p.Ser301=
NM_001282678.1:c.277T= NP_001269607.1:p.Ser93=
XR_242246.3:n.997T=
XM_017012319.2:c.-766T= XP_016867808.1:n.-766T=
XR_001744808.2:n.11T=
XR_242246.5:n.948T=
NM_000466.3:c.901T= MANE Select NP_000457.1:p.Ser301=
NM_001282677.2:c.901T= NP_001269606.1:p.Ser301=
NM_001282678.2:c.277T= NP_001269607.1:p.Ser93=