Canonical Allele Identifier: CA1725931493

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494551T= , CM000669.2:g.92494551T= GRCh38
NC_000007.13:g.92123865T= , CM000669.1:g.92123865T= GRCh37
NC_000007.12:g.91961801T= NCBI36
NG_008341.1:g.38981A=
NG_008341.2:g.38981A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2862A= (PEX1) MANE Select ENSP00000248633.4:p.Thr954=
ENST00000248633.8:c.2862A= (PEX1) ENSP00000248633.4:p.Thr954=
ENST00000428214.5:c.2691A= (PEX1) ENSP00000394413.1:p.Thr897=
ENST00000438045.5:c.1896A= (PEX1) ENSP00000410438.1:p.Thr632=
ENST00000484913.5:n.2901A= (PEX1)
ENST00000496420.5:n.2754A= (PEX1)
NM_000466.2:c.2862A= (PEX1) NP_000457.1:p.Thr954=
NM_001282677.1:c.2691A= (PEX1) NP_001269606.1:p.Thr897=
NM_001282678.1:c.2238A= (PEX1) NP_001269607.1:p.Thr746=
XM_005250433.3:c.1113A= (PEX1) XP_005250490.1:p.Thr371=
XR_242246.3:n.2958A= (PEX1)
XM_017012319.2:c.1113A= (PEX1) XP_016867808.1:p.Thr371=
XR_001744808.2:n.1889A= (PEX1)
XR_001744843.2:n.5520T= (GATAD1)
XR_242246.5:n.2909A= (PEX1)
XR_927494.3:n.4371T= (GATAD1)
XR_927503.3:n.4302T= (GATAD1)
NM_000466.3:c.2862A= (PEX1) MANE Select NP_000457.1:p.Thr954=
NM_001282677.2:c.2691A= (PEX1) NP_001269606.1:p.Thr897=
NM_001282678.2:c.2238A= (PEX1) NP_001269607.1:p.Thr746=