Canonical Allele Identifier: CA1725936121
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92501999C= , CM000669.2:g.92501999C= GRCh38
NC_000007.13:g.92131313C= , CM000669.1:g.92131313C= GRCh37
NC_000007.12:g.91969249C= NCBI36
NG_008341.1:g.31533G=
NG_008341.2:g.31533G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2307G= MANE Select ENSP00000248633.4:p.Leu769=
ENST00000248633.8:c.2307G= ENSP00000248633.4:p.Leu769=
ENST00000428214.5:c.2136G= ENSP00000394413.1:p.Leu712=
ENST00000438045.5:c.1341G= ENSP00000410438.1:p.Leu447=
ENST00000484913.5:n.2346G=
ENST00000496092.1:n.105G=
ENST00000496420.5:n.1983G=
NM_000466.2:c.2307G= NP_000457.1:p.Leu769=
NM_001282677.1:c.2136G= NP_001269606.1:p.Leu712=
NM_001282678.1:c.1683G= NP_001269607.1:p.Leu561=
XM_005250433.3:c.558G= XP_005250490.1:p.Leu186=
XR_242246.3:n.2403G=
XM_017012319.2:c.558G= XP_016867808.1:p.Leu186=
XR_001744808.2:n.1334G=
XR_242246.5:n.2354G=
NM_000466.3:c.2307G= MANE Select NP_000457.1:p.Leu769=
NM_001282677.2:c.2136G= NP_001269606.1:p.Leu712=
NM_001282678.2:c.1683G= NP_001269607.1:p.Leu561=