Canonical Allele Identifier: CA368159552
ClinVar RCV:
ClinVar Variation:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489350G>T , CM000669.2:g.92489350G>T GRCh38
NC_000007.13:g.92118664G>T , CM000669.1:g.92118664G>T GRCh37
NC_000007.12:g.91956600G>T NCBI36
NG_008341.1:g.44182C>A
NG_008341.2:g.44182C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3710C>A (PEX1) MANE Select ENSP00000248633.4:p.Ala1237Glu
ENST00000248633.8:c.3710C>A (PEX1) ENSP00000248633.4:p.Ala1237Glu
ENST00000428214.5:c.3539C>A (PEX1) ENSP00000394413.1:p.Ala1180Glu
ENST00000438045.5:c.2744C>A (PEX1) ENSP00000410438.1:p.Ala915Glu
ENST00000477342.1:n.445C>A (PEX1)
ENST00000484913.5:n.3749C>A (PEX1)
ENST00000496420.5:n.4760C>A (PEX1)
NM_000466.2:c.3710C>A (PEX1) NP_000457.1:p.Ala1237Glu
NM_001282677.1:c.3539C>A (PEX1) NP_001269606.1:p.Ala1180Glu
NM_001282678.1:c.3086C>A (PEX1) NP_001269607.1:p.Ala1029Glu
XM_005250433.3:c.1961C>A (PEX1) XP_005250490.1:p.Ala654Glu
XR_242246.3:n.3801C>A (PEX1)
XR_927494.1:n.1036-1893G>T (GATAD1)
XR_927495.1:n.1036-736G>T (GATAD1)
XR_927496.1:n.1041-1893G>T (GATAD1)
XR_927497.1:n.1036-736G>T (GATAD1)
XR_927498.1:n.1124-1893G>T (GATAD1)
XR_927500.1:n.1033-1893G>T (GATAD1)
XR_927502.1:n.1033-736G>T (GATAD1)
XR_927503.1:n.967-1893G>T (GATAD1)
XM_017012319.2:c.1961C>A (PEX1) XP_016867808.1:p.Ala654Glu
XR_001744808.2:n.2732C>A (PEX1)
XR_001744842.2:n.2281-1893G>T (GATAD1)
XR_001744843.2:n.2212-1893G>T (GATAD1)
XR_002956472.1:n.2281-736G>T (GATAD1)
XR_002956473.1:n.2369-1893G>T (GATAD1)
XR_002956474.1:n.2286-1893G>T (GATAD1)
XR_242246.5:n.3752C>A (PEX1)
XR_927494.3:n.1063-1893G>T (GATAD1)
XR_927500.3:n.1060-1893G>T (GATAD1)
XR_927503.3:n.994-1893G>T (GATAD1)
NM_000466.3:c.3710C>A (PEX1) MANE Select NP_000457.1:p.Ala1237Glu
NM_001282677.2:c.3539C>A (PEX1) NP_001269606.1:p.Ala1180Glu
NM_001282678.2:c.3086C>A (PEX1) NP_001269607.1:p.Ala1029Glu