Canonical Allele Identifier: CA368159802
Community Standard Title: NM_000466.3(PEX1):c.3691C>T (p.Gln1231Ter)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489369G>A , CM000669.2:g.92489369G>A GRCh38
NC_000007.13:g.92118683G>A , CM000669.1:g.92118683G>A GRCh37
NC_000007.12:g.91956619G>A NCBI36
NG_008341.1:g.44163C>T
NG_008341.2:g.44163C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000466.3:c.3691C>T (PEX1) MANE Select NP_000457.1:p.Gln1231Ter
ENST00000248633.9:c.3691C>T (PEX1) MANE Select ENSP00000248633.4:p.Gln1231Ter
NM_000466.2:c.3691C>T (PEX1) NP_000457.1:p.Gln1231Ter
NM_001282677.1:c.3520C>T (PEX1) NP_001269606.1:p.Gln1174Ter
NM_001282677.2:c.3520C>T (PEX1) NP_001269606.1:p.Gln1174Ter
NM_001282678.1:c.3067C>T (PEX1) NP_001269607.1:p.Gln1023Ter
NM_001282678.2:c.3067C>T (PEX1) NP_001269607.1:p.Gln1023Ter
ENST00000248633.8:c.3691C>T (PEX1) ENSP00000248633.4:p.Gln1231Ter
ENST00000428214.5:c.3520C>T (PEX1) ENSP00000394413.1:p.Gln1174Ter
ENST00000438045.5:c.2725C>T (PEX1) ENSP00000410438.1:p.Gln909Ter
ENST00000477342.1:n.426C>T (PEX1)
ENST00000484913.5:n.3730C>T (PEX1)
ENST00000496420.5:n.4741C>T (PEX1)
XM_005250433.3:c.1942C>T (PEX1) XP_005250490.1:p.Gln648Ter
XM_017012319.2:c.1942C>T (PEX1) XP_016867808.1:p.Gln648Ter
XR_001744808.2:n.2713C>T (PEX1)
XR_001744842.2:n.2281-1874G>A (GATAD1)
XR_001744843.2:n.2212-1874G>A (GATAD1)
XR_002956472.1:n.2281-717G>A (GATAD1)
XR_002956473.1:n.2369-1874G>A (GATAD1)
XR_002956474.1:n.2286-1874G>A (GATAD1)
XR_242246.3:n.3782C>T (PEX1)
XR_242246.5:n.3733C>T (PEX1)
XR_927494.1:n.1036-1874G>A (GATAD1)
XR_927494.3:n.1063-1874G>A (GATAD1)
XR_927495.1:n.1036-717G>A (GATAD1)
XR_927496.1:n.1041-1874G>A (GATAD1)
XR_927497.1:n.1036-717G>A (GATAD1)
XR_927498.1:n.1124-1874G>A (GATAD1)
XR_927500.1:n.1033-1874G>A (GATAD1)
XR_927500.3:n.1060-1874G>A (GATAD1)
XR_927502.1:n.1033-717G>A (GATAD1)
XR_927503.1:n.967-1874G>A (GATAD1)
XR_927503.3:n.994-1874G>A (GATAD1)