Canonical Allele Identifier: CA1725939068
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92504873G= , CM000669.2:g.92504873G= GRCh38
NC_000007.13:g.92134187G= , CM000669.1:g.92134187G= GRCh37
NC_000007.12:g.91972123G= NCBI36
NG_008341.1:g.28659C=
NG_008341.2:g.28659C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.1930C= MANE Select ENSP00000248633.4:p.Leu644=
ENST00000248633.8:c.1930C= ENSP00000248633.4:p.Leu644=
ENST00000428214.5:c.1900+1375C= ENSP00000394413.1:n.1900+1375C=
ENST00000438045.5:c.964C= ENSP00000410438.1:p.Leu322=
ENST00000484913.5:n.1969C=
ENST00000496420.5:n.1606C=
NM_000466.2:c.1930C= NP_000457.1:p.Leu644=
NM_001282677.1:c.1900+1375C= NP_001269606.1:n.1900+1375C=
NM_001282678.1:c.1306C= NP_001269607.1:p.Leu436=
XM_005250433.3:c.181C= XP_005250490.1:p.Leu61=
XR_242246.3:n.2026C=
XM_017012319.2:c.181C= XP_016867808.1:p.Leu61=
XR_001744808.2:n.957C=
XR_242246.5:n.1977C=
NM_000466.3:c.1930C= MANE Select NP_000457.1:p.Leu644=
NM_001282677.2:c.1900+1375C= NP_001269606.1:n.1900+1375C=
NM_001282678.2:c.1306C= NP_001269607.1:p.Leu436=