Canonical Allele Identifier: CA368168543

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92494550C>G , CM000669.2:g.92494550C>G GRCh38
NC_000007.13:g.92123864C>G , CM000669.1:g.92123864C>G GRCh37
NC_000007.12:g.91961800C>G NCBI36
NG_008341.1:g.38982G>C
NG_008341.2:g.38982G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.2863G>C (PEX1) MANE Select ENSP00000248633.4:p.Gly955Arg
ENST00000248633.8:c.2863G>C (PEX1) ENSP00000248633.4:p.Gly955Arg
ENST00000428214.5:c.2692G>C (PEX1) ENSP00000394413.1:p.Gly898Arg
ENST00000438045.5:c.1897G>C (PEX1) ENSP00000410438.1:p.Gly633Arg
ENST00000484913.5:n.2902G>C (PEX1)
ENST00000496420.5:n.2755G>C (PEX1)
NM_000466.2:c.2863G>C (PEX1) NP_000457.1:p.Gly955Arg
NM_001282677.1:c.2692G>C (PEX1) NP_001269606.1:p.Gly898Arg
NM_001282678.1:c.2239G>C (PEX1) NP_001269607.1:p.Gly747Arg
XM_005250433.3:c.1114G>C (PEX1) XP_005250490.1:p.Gly372Arg
XR_242246.3:n.2959G>C (PEX1)
XM_017012319.2:c.1114G>C (PEX1) XP_016867808.1:p.Gly372Arg
XR_001744808.2:n.1890G>C (PEX1)
XR_001744843.2:n.5519C>G (GATAD1)
XR_242246.5:n.2910G>C (PEX1)
XR_927494.3:n.4370C>G (GATAD1)
XR_927503.3:n.4301C>G (GATAD1)
NM_000466.3:c.2863G>C (PEX1) MANE Select NP_000457.1:p.Gly955Arg
NM_001282677.2:c.2692G>C (PEX1) NP_001269606.1:p.Gly898Arg
NM_001282678.2:c.2239G>C (PEX1) NP_001269607.1:p.Gly747Arg