Canonical Allele Identifier: CA368164515

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92491444T>C , CM000669.2:g.92491444T>C GRCh38
NC_000007.13:g.92120758T>C , CM000669.1:g.92120758T>C GRCh37
NC_000007.12:g.91958694T>C NCBI36
NG_008341.1:g.42088A>G
NG_008341.2:g.42088A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3266A>G (PEX1) MANE Select ENSP00000248633.4:p.His1089Arg
ENST00000248633.8:c.3266A>G (PEX1) ENSP00000248633.4:p.His1089Arg
ENST00000428214.5:c.3095A>G (PEX1) ENSP00000394413.1:p.His1032Arg
ENST00000438045.5:c.2300A>G (PEX1) ENSP00000410438.1:p.His767Arg
ENST00000484913.5:n.3305A>G (PEX1)
ENST00000496420.5:n.4321A>G (PEX1)
NM_000466.2:c.3266A>G (PEX1) NP_000457.1:p.His1089Arg
NM_001282677.1:c.3095A>G (PEX1) NP_001269606.1:p.His1032Arg
NM_001282678.1:c.2642A>G (PEX1) NP_001269607.1:p.His881Arg
XM_005250433.3:c.1517A>G (PEX1) XP_005250490.1:p.His506Arg
XR_242246.3:n.3362A>G (PEX1)
XM_017012319.2:c.1517A>G (PEX1) XP_016867808.1:p.His506Arg
XR_001744808.2:n.2293A>G (PEX1)
XR_001744842.2:n.2482T>C (GATAD1)
XR_001744843.2:n.2413T>C (GATAD1)
XR_002956472.1:n.2539T>C (GATAD1)
XR_002956473.1:n.2570T>C (GATAD1)
XR_002956474.1:n.2487T>C (GATAD1)
XR_242246.5:n.3313A>G (PEX1)
XR_927494.3:n.1264T>C (GATAD1)
XR_927500.3:n.1261T>C (GATAD1)
XR_927503.3:n.1195T>C (GATAD1)
NM_000466.3:c.3266A>G (PEX1) MANE Select NP_000457.1:p.His1089Arg
NM_001282677.2:c.3095A>G (PEX1) NP_001269606.1:p.His1032Arg
NM_001282678.2:c.2642A>G (PEX1) NP_001269607.1:p.His881Arg