Canonical Allele Identifier: CA368164551

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491447T>G , CM000669.2:g.92491447T>G GRCh38
NC_000007.13:g.92120761T>G , CM000669.1:g.92120761T>G GRCh37
NC_000007.12:g.91958697T>G NCBI36
NG_008341.1:g.42085A>C
NG_008341.2:g.42085A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3263A>C (PEX1) MANE Select ENSP00000248633.4:p.Asn1088Thr
ENST00000248633.8:c.3263A>C (PEX1) ENSP00000248633.4:p.Asn1088Thr
ENST00000428214.5:c.3092A>C (PEX1) ENSP00000394413.1:p.Asn1031Thr
ENST00000438045.5:c.2297A>C (PEX1) ENSP00000410438.1:p.Asn766Thr
ENST00000484913.5:n.3302A>C (PEX1)
ENST00000496420.5:n.4318A>C (PEX1)
NM_000466.2:c.3263A>C (PEX1) NP_000457.1:p.Asn1088Thr
NM_001282677.1:c.3092A>C (PEX1) NP_001269606.1:p.Asn1031Thr
NM_001282678.1:c.2639A>C (PEX1) NP_001269607.1:p.Asn880Thr
XM_005250433.3:c.1514A>C (PEX1) XP_005250490.1:p.Asn505Thr
XR_242246.3:n.3359A>C (PEX1)
XM_017012319.2:c.1514A>C (PEX1) XP_016867808.1:p.Asn505Thr
XR_001744808.2:n.2290A>C (PEX1)
XR_001744842.2:n.2485T>G (GATAD1)
XR_001744843.2:n.2416T>G (GATAD1)
XR_002956472.1:n.2542T>G (GATAD1)
XR_002956473.1:n.2573T>G (GATAD1)
XR_002956474.1:n.2490T>G (GATAD1)
XR_242246.5:n.3310A>C (PEX1)
XR_927494.3:n.1267T>G (GATAD1)
XR_927500.3:n.1264T>G (GATAD1)
XR_927503.3:n.1198T>G (GATAD1)
NM_000466.3:c.3263A>C (PEX1) MANE Select NP_000457.1:p.Asn1088Thr
NM_001282677.2:c.3092A>C (PEX1) NP_001269606.1:p.Asn1031Thr
NM_001282678.2:c.2639A>C (PEX1) NP_001269607.1:p.Asn880Thr