Canonical Allele Identifier: CA368159504

Linked Data

gnomAD v4: 7-92489344-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92489344C>T , CM000669.2:g.92489344C>T GRCh38
NC_000007.13:g.92118658C>T , CM000669.1:g.92118658C>T GRCh37
NC_000007.12:g.91956594C>T NCBI36
NG_008341.1:g.44188G>A
NG_008341.2:g.44188G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.3716G>A (PEX1) MANE Select ENSP00000248633.4:p.Gly1239Asp
ENST00000248633.8:c.3716G>A (PEX1) ENSP00000248633.4:p.Gly1239Asp
ENST00000428214.5:c.3545G>A (PEX1) ENSP00000394413.1:p.Gly1182Asp
ENST00000438045.5:c.2750G>A (PEX1) ENSP00000410438.1:p.Gly917Asp
ENST00000477342.1:n.451G>A (PEX1)
ENST00000484913.5:n.3755G>A (PEX1)
ENST00000496420.5:n.4766G>A (PEX1)
NM_000466.2:c.3716G>A (PEX1) NP_000457.1:p.Gly1239Asp
NM_001282677.1:c.3545G>A (PEX1) NP_001269606.1:p.Gly1182Asp
NM_001282678.1:c.3092G>A (PEX1) NP_001269607.1:p.Gly1031Asp
XM_005250433.3:c.1967G>A (PEX1) XP_005250490.1:p.Gly656Asp
XR_242246.3:n.3807G>A (PEX1)
XR_927494.1:n.1036-1899C>T (GATAD1)
XR_927495.1:n.1036-742C>T (GATAD1)
XR_927496.1:n.1041-1899C>T (GATAD1)
XR_927497.1:n.1036-742C>T (GATAD1)
XR_927498.1:n.1124-1899C>T (GATAD1)
XR_927500.1:n.1033-1899C>T (GATAD1)
XR_927502.1:n.1033-742C>T (GATAD1)
XR_927503.1:n.967-1899C>T (GATAD1)
XM_017012319.2:c.1967G>A (PEX1) XP_016867808.1:p.Gly656Asp
XR_001744808.2:n.2738G>A (PEX1)
XR_001744842.2:n.2281-1899C>T (GATAD1)
XR_001744843.2:n.2212-1899C>T (GATAD1)
XR_002956472.1:n.2281-742C>T (GATAD1)
XR_002956473.1:n.2369-1899C>T (GATAD1)
XR_002956474.1:n.2286-1899C>T (GATAD1)
XR_242246.5:n.3758G>A (PEX1)
XR_927494.3:n.1063-1899C>T (GATAD1)
XR_927500.3:n.1060-1899C>T (GATAD1)
XR_927503.3:n.994-1899C>T (GATAD1)
NM_000466.3:c.3716G>A (PEX1) MANE Select NP_000457.1:p.Gly1239Asp
NM_001282677.2:c.3545G>A (PEX1) NP_001269606.1:p.Gly1182Asp
NM_001282678.2:c.3092G>A (PEX1) NP_001269607.1:p.Gly1031Asp