Canonical Allele Identifier: CA1725933396
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92496769C= , CM000669.2:g.92496769C= GRCh38
NC_000007.13:g.92126083C= , CM000669.1:g.92126083C= GRCh37
NC_000007.12:g.91964019C= NCBI36
NG_008341.1:g.36763G=
NG_008341.2:g.36763G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2727G= MANE Select ENSP00000248633.4:p.Glu909=
ENST00000248633.8:c.2727G= ENSP00000248633.4:p.Glu909=
ENST00000428214.5:c.2556G= ENSP00000394413.1:p.Glu852=
ENST00000438045.5:c.1761G= ENSP00000410438.1:p.Glu587=
ENST00000484913.5:n.2766G=
ENST00000496420.5:n.2619G=
NM_000466.2:c.2727G= NP_000457.1:p.Glu909=
NM_001282677.1:c.2556G= NP_001269606.1:p.Glu852=
NM_001282678.1:c.2103G= NP_001269607.1:p.Glu701=
XM_005250433.3:c.978G= XP_005250490.1:p.Glu326=
XR_242246.3:n.2823G=
XM_017012319.2:c.978G= XP_016867808.1:p.Glu326=
XR_001744808.2:n.1754G=
XR_242246.5:n.2774G=
NM_000466.3:c.2727G= MANE Select NP_000457.1:p.Glu909=
NM_001282677.2:c.2556G= NP_001269606.1:p.Glu852=
NM_001282678.2:c.2103G= NP_001269607.1:p.Glu701=