Canonical Allele Identifier: CA1725931460

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494538G= , CM000669.2:g.92494538G= GRCh38
NC_000007.13:g.92123852G= , CM000669.1:g.92123852G= GRCh37
NC_000007.12:g.91961788G= NCBI36
NG_008341.1:g.38994C=
NG_008341.2:g.38994C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2875C= (PEX1) MANE Select ENSP00000248633.4:p.Arg959=
ENST00000248633.8:c.2875C= (PEX1) ENSP00000248633.4:p.Arg959=
ENST00000428214.5:c.2704C= (PEX1) ENSP00000394413.1:p.Arg902=
ENST00000438045.5:c.1909C= (PEX1) ENSP00000410438.1:p.Arg637=
ENST00000484913.5:n.2914C= (PEX1)
ENST00000496420.5:n.2767C= (PEX1)
NM_000466.2:c.2875C= (PEX1) NP_000457.1:p.Arg959=
NM_001282677.1:c.2704C= (PEX1) NP_001269606.1:p.Arg902=
NM_001282678.1:c.2251C= (PEX1) NP_001269607.1:p.Arg751=
XM_005250433.3:c.1126C= (PEX1) XP_005250490.1:p.Arg376=
XR_242246.3:n.2971C= (PEX1)
XM_017012319.2:c.1126C= (PEX1) XP_016867808.1:p.Arg376=
XR_001744808.2:n.1902C= (PEX1)
XR_001744843.2:n.5507G= (GATAD1)
XR_242246.5:n.2922C= (PEX1)
XR_927494.3:n.4358G= (GATAD1)
XR_927503.3:n.4289G= (GATAD1)
NM_000466.3:c.2875C= (PEX1) MANE Select NP_000457.1:p.Arg959=
NM_001282677.2:c.2704C= (PEX1) NP_001269606.1:p.Arg902=
NM_001282678.2:c.2251C= (PEX1) NP_001269607.1:p.Arg751=