Canonical Allele Identifier: CA1725931049

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494318C= , CM000669.2:g.92494318C= GRCh38
NC_000007.13:g.92123632C= , CM000669.1:g.92123632C= GRCh37
NC_000007.12:g.91961568C= NCBI36
NG_008341.1:g.39214G=
NG_008341.2:g.39214G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3005G= (PEX1) MANE Select ENSP00000248633.4:p.Cys1002=
ENST00000248633.8:c.3005G= (PEX1) ENSP00000248633.4:p.Cys1002=
ENST00000428214.5:c.2834G= (PEX1) ENSP00000394413.1:p.Cys945=
ENST00000438045.5:c.2039G= (PEX1) ENSP00000410438.1:p.Cys680=
ENST00000484913.5:n.3044G= (PEX1)
ENST00000496420.5:n.2897G= (PEX1)
NM_000466.2:c.3005G= (PEX1) NP_000457.1:p.Cys1002=
NM_001282677.1:c.2834G= (PEX1) NP_001269606.1:p.Cys945=
NM_001282678.1:c.2381G= (PEX1) NP_001269607.1:p.Cys794=
XM_005250433.3:c.1256G= (PEX1) XP_005250490.1:p.Cys419=
XR_242246.3:n.3101G= (PEX1)
XM_017012319.2:c.1256G= (PEX1) XP_016867808.1:p.Cys419=
XR_001744808.2:n.2032G= (PEX1)
XR_001744843.2:n.5287C= (GATAD1)
XR_242246.5:n.3052G= (PEX1)
XR_927494.3:n.4138C= (GATAD1)
XR_927503.3:n.4069C= (GATAD1)
NM_000466.3:c.3005G= (PEX1) MANE Select NP_000457.1:p.Cys1002=
NM_001282677.2:c.2834G= (PEX1) NP_001269606.1:p.Cys945=
NM_001282678.2:c.2381G= (PEX1) NP_001269607.1:p.Cys794=