Canonical Allele Identifier: CA368167255

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494293C>G , CM000669.2:g.92494293C>G GRCh38
NC_000007.13:g.92123607C>G , CM000669.1:g.92123607C>G GRCh37
NC_000007.12:g.91961543C>G NCBI36
NG_008341.1:g.39239G>C
NG_008341.2:g.39239G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3030G>C (PEX1) MANE Select ENSP00000248633.4:p.Gln1010His
ENST00000248633.8:c.3030G>C (PEX1) ENSP00000248633.4:p.Gln1010His
ENST00000428214.5:c.2859G>C (PEX1) ENSP00000394413.1:p.Gln953His
ENST00000438045.5:c.2064G>C (PEX1) ENSP00000410438.1:p.Gln688His
ENST00000484913.5:n.3069G>C (PEX1)
ENST00000496420.5:n.2922G>C (PEX1)
NM_000466.2:c.3030G>C (PEX1) NP_000457.1:p.Gln1010His
NM_001282677.1:c.2859G>C (PEX1) NP_001269606.1:p.Gln953His
NM_001282678.1:c.2406G>C (PEX1) NP_001269607.1:p.Gln802His
XM_005250433.3:c.1281G>C (PEX1) XP_005250490.1:p.Gln427His
XR_242246.3:n.3126G>C (PEX1)
XM_017012319.2:c.1281G>C (PEX1) XP_016867808.1:p.Gln427His
XR_001744808.2:n.2057G>C (PEX1)
XR_001744843.2:n.5262C>G (GATAD1)
XR_242246.5:n.3077G>C (PEX1)
XR_927494.3:n.4113C>G (GATAD1)
XR_927503.3:n.4044C>G (GATAD1)
NM_000466.3:c.3030G>C (PEX1) MANE Select NP_000457.1:p.Gln1010His
NM_001282677.2:c.2859G>C (PEX1) NP_001269606.1:p.Gln953His
NM_001282678.2:c.2406G>C (PEX1) NP_001269607.1:p.Gln802His