Canonical Allele Identifier: CA368161453

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489787A>C , CM000669.2:g.92489787A>C GRCh38
NC_000007.13:g.92119101A>C , CM000669.1:g.92119101A>C GRCh37
NC_000007.12:g.91957037A>C NCBI36
NG_008341.1:g.43745T>G
NG_008341.2:g.43745T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3563T>G (PEX1) MANE Select ENSP00000248633.4:p.Leu1188Arg
ENST00000248633.8:c.3563T>G (PEX1) ENSP00000248633.4:p.Leu1188Arg
ENST00000428214.5:n.3392T>G (PEX1) ENSP00000394413.1:p.Leu1131Arg
ENST00000438045.5:c.2597T>G (PEX1) ENSP00000410438.1:p.Leu866Arg
ENST00000469417.1:n.460T>G (PEX1)
ENST00000477342.1:n.8T>G (PEX1)
ENST00000484913.5:n.3602T>G (PEX1)
ENST00000496420.5:n.4618T>G (PEX1)
NM_000466.2:c.3563T>G (PEX1) NP_000457.1:p.Leu1188Arg
NM_001282677.1:c.3392T>G (PEX1) NP_001269606.1:p.Leu1131Arg
NM_001282678.1:c.2939T>G (PEX1) NP_001269607.1:p.Leu980Arg
XM_005250433.3:c.1814T>G (PEX1) XP_005250490.1:p.Leu605Arg
XR_242246.3:n.3659T>G (PEX1)
XR_927494.1:n.1036-1456A>C (GATAD1)
XR_927495.1:n.1036-299A>C (GATAD1)
XR_927496.1:n.1041-1456A>C (GATAD1)
XR_927497.1:n.1036-299A>C (GATAD1)
XR_927498.1:n.1124-1456A>C (GATAD1)
XR_927500.1:n.1033-1456A>C (GATAD1)
XR_927502.1:n.1033-299A>C (GATAD1)
XR_927503.1:n.967-1456A>C (GATAD1)
XM_017012319.2:c.1814T>G (PEX1) XP_016867808.1:p.Leu605Arg
XR_001744808.2:n.2590T>G (PEX1)
XR_001744842.2:n.2281-1456A>C (GATAD1)
XR_001744843.2:n.2212-1456A>C (GATAD1)
XR_002956472.1:n.2281-299A>C (GATAD1)
XR_002956473.1:n.2369-1456A>C (GATAD1)
XR_002956474.1:n.2286-1456A>C (GATAD1)
XR_242246.5:n.3610T>G (PEX1)
XR_927494.3:n.1063-1456A>C (GATAD1)
XR_927500.3:n.1060-1456A>C (GATAD1)
XR_927503.3:n.994-1456A>C (GATAD1)
NM_000466.3:c.3563T>G (PEX1) MANE Select NP_000457.1:p.Leu1188Arg
NM_001282677.2:c.3392T>G (PEX1) NP_001269606.1:p.Leu1131Arg
NM_001282678.2:c.2939T>G (PEX1) NP_001269607.1:p.Leu980Arg