Canonical Allele Identifier: CA1725931068

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494330C= , CM000669.2:g.92494330C= GRCh38
NC_000007.13:g.92123644C= , CM000669.1:g.92123644C= GRCh37
NC_000007.12:g.91961580C= NCBI36
NG_008341.1:g.39202G=
NG_008341.2:g.39202G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2993G= (PEX1) MANE Select ENSP00000248633.4:p.Arg998=
ENST00000248633.8:c.2993G= (PEX1) ENSP00000248633.4:p.Arg998=
ENST00000428214.5:c.2822G= (PEX1) ENSP00000394413.1:p.Arg941=
ENST00000438045.5:c.2027G= (PEX1) ENSP00000410438.1:p.Arg676=
ENST00000484913.5:n.3032G= (PEX1)
ENST00000496420.5:n.2885G= (PEX1)
NM_000466.2:c.2993G= (PEX1) NP_000457.1:p.Arg998=
NM_001282677.1:c.2822G= (PEX1) NP_001269606.1:p.Arg941=
NM_001282678.1:c.2369G= (PEX1) NP_001269607.1:p.Arg790=
XM_005250433.3:c.1244G= (PEX1) XP_005250490.1:p.Arg415=
XR_242246.3:n.3089G= (PEX1)
XM_017012319.2:c.1244G= (PEX1) XP_016867808.1:p.Arg415=
XR_001744808.2:n.2020G= (PEX1)
XR_001744843.2:n.5299C= (GATAD1)
XR_242246.5:n.3040G= (PEX1)
XR_927494.3:n.4150C= (GATAD1)
XR_927503.3:n.4081C= (GATAD1)
NM_000466.3:c.2993G= (PEX1) MANE Select NP_000457.1:p.Arg998=
NM_001282677.2:c.2822G= (PEX1) NP_001269606.1:p.Arg941=
NM_001282678.2:c.2369G= (PEX1) NP_001269607.1:p.Arg790=