Canonical Allele Identifier: CA1725947264
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517404T= , CM000669.2:g.92517404T= GRCh38
NC_000007.13:g.92146718T= , CM000669.1:g.92146718T= GRCh37
NC_000007.12:g.91984654T= NCBI36
NG_008341.1:g.16128A=
NG_008341.2:g.16128A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1111A= MANE Select ENSP00000248633.4:p.Arg371=
ENST00000248633.8:c.1111A= ENSP00000248633.4:p.Arg371=
ENST00000422866.1:c.12A=
ENST00000428214.5:c.1111A= ENSP00000394413.1:p.Arg371=
ENST00000438045.5:c.274-3437A= ENSP00000410438.1:n.274-3437A=
ENST00000484913.5:n.1150A=
NM_000466.2:c.1111A= NP_000457.1:p.Arg371=
NM_001282677.1:c.1111A= NP_001269606.1:p.Arg371=
NM_001282678.1:c.487A= NP_001269607.1:p.Arg163=
XR_242246.3:n.1207A=
XM_017012319.2:c.-556A= XP_016867808.1:n.-556A=
XR_001744808.2:n.221A=
XR_242246.5:n.1158A=
NM_000466.3:c.1111A= MANE Select NP_000457.1:p.Arg371=
NM_001282677.2:c.1111A= NP_001269606.1:p.Arg371=
NM_001282678.2:c.487A= NP_001269607.1:p.Arg163=