Canonical Allele Identifier: CA1725931142

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494369C= , CM000669.2:g.92494369C= GRCh38
NC_000007.13:g.92123683C= , CM000669.1:g.92123683C= GRCh37
NC_000007.12:g.91961619C= NCBI36
NG_008341.1:g.39163G=
NG_008341.2:g.39163G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2954G= (PEX1) MANE Select ENSP00000248633.4:p.Arg985=
ENST00000248633.8:c.2954G= (PEX1) ENSP00000248633.4:p.Arg985=
ENST00000428214.5:c.2783G= (PEX1) ENSP00000394413.1:p.Arg928=
ENST00000438045.5:c.1988G= (PEX1) ENSP00000410438.1:p.Arg663=
ENST00000484913.5:n.2993G= (PEX1)
ENST00000496420.5:n.2846G= (PEX1)
NM_000466.2:c.2954G= (PEX1) NP_000457.1:p.Arg985=
NM_001282677.1:c.2783G= (PEX1) NP_001269606.1:p.Arg928=
NM_001282678.1:c.2330G= (PEX1) NP_001269607.1:p.Arg777=
XM_005250433.3:c.1205G= (PEX1) XP_005250490.1:p.Arg402=
XR_242246.3:n.3050G= (PEX1)
XM_017012319.2:c.1205G= (PEX1) XP_016867808.1:p.Arg402=
XR_001744808.2:n.1981G= (PEX1)
XR_001744843.2:n.5338C= (GATAD1)
XR_242246.5:n.3001G= (PEX1)
XR_927494.3:n.4189C= (GATAD1)
XR_927503.3:n.4120C= (GATAD1)
NM_000466.3:c.2954G= (PEX1) MANE Select NP_000457.1:p.Arg985=
NM_001282677.2:c.2783G= (PEX1) NP_001269606.1:p.Arg928=
NM_001282678.2:c.2330G= (PEX1) NP_001269607.1:p.Arg777=