Canonical Allele Identifier: CA368161472

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489788G>T , CM000669.2:g.92489788G>T GRCh38
NC_000007.13:g.92119102G>T , CM000669.1:g.92119102G>T GRCh37
NC_000007.12:g.91957038G>T NCBI36
NG_008341.1:g.43744C>A
NG_008341.2:g.43744C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.3562C>A (PEX1) MANE Select ENSP00000248633.4:p.Leu1188Ile
ENST00000248633.8:c.3562C>A (PEX1) ENSP00000248633.4:p.Leu1188Ile
ENST00000428214.5:n.3391C>A (PEX1) ENSP00000394413.1:p.Leu1131Ile
ENST00000438045.5:c.2596C>A (PEX1) ENSP00000410438.1:p.Leu866Ile
ENST00000469417.1:n.459C>A (PEX1)
ENST00000477342.1:n.7C>A (PEX1)
ENST00000484913.5:n.3601C>A (PEX1)
ENST00000496420.5:n.4617C>A (PEX1)
NM_000466.2:c.3562C>A (PEX1) NP_000457.1:p.Leu1188Ile
NM_001282677.1:c.3391C>A (PEX1) NP_001269606.1:p.Leu1131Ile
NM_001282678.1:c.2938C>A (PEX1) NP_001269607.1:p.Leu980Ile
XM_005250433.3:c.1813C>A (PEX1) XP_005250490.1:p.Leu605Ile
XR_242246.3:n.3658C>A (PEX1)
XR_927494.1:n.1036-1455G>T (GATAD1)
XR_927495.1:n.1036-298G>T (GATAD1)
XR_927496.1:n.1041-1455G>T (GATAD1)
XR_927497.1:n.1036-298G>T (GATAD1)
XR_927498.1:n.1124-1455G>T (GATAD1)
XR_927500.1:n.1033-1455G>T (GATAD1)
XR_927502.1:n.1033-298G>T (GATAD1)
XR_927503.1:n.967-1455G>T (GATAD1)
XM_017012319.2:c.1813C>A (PEX1) XP_016867808.1:p.Leu605Ile
XR_001744808.2:n.2589C>A (PEX1)
XR_001744842.2:n.2281-1455G>T (GATAD1)
XR_001744843.2:n.2212-1455G>T (GATAD1)
XR_002956472.1:n.2281-298G>T (GATAD1)
XR_002956473.1:n.2369-1455G>T (GATAD1)
XR_002956474.1:n.2286-1455G>T (GATAD1)
XR_242246.5:n.3609C>A (PEX1)
XR_927494.3:n.1063-1455G>T (GATAD1)
XR_927500.3:n.1060-1455G>T (GATAD1)
XR_927503.3:n.994-1455G>T (GATAD1)
NM_000466.3:c.3562C>A (PEX1) MANE Select NP_000457.1:p.Leu1188Ile
NM_001282677.2:c.3391C>A (PEX1) NP_001269606.1:p.Leu1131Ile
NM_001282678.2:c.2938C>A (PEX1) NP_001269607.1:p.Leu980Ile