Canonical Allele Identifier: CA1725935197
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92499815C= , CM000669.2:g.92499815C= GRCh38
NC_000007.13:g.92129129C= , CM000669.1:g.92129129C= GRCh37
NC_000007.12:g.91967065C= NCBI36
NG_008341.1:g.33717G=
NG_008341.2:g.33717G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2607G= MANE Select ENSP00000248633.4:p.Leu869=
ENST00000248633.8:c.2607G= ENSP00000248633.4:p.Leu869=
ENST00000428214.5:c.2436G= ENSP00000394413.1:p.Leu812=
ENST00000438045.5:c.1641G= ENSP00000410438.1:p.Leu547=
ENST00000484913.5:n.2646G=
ENST00000496420.5:n.2499G=
NM_000466.2:c.2607G= NP_000457.1:p.Leu869=
NM_001282677.1:c.2436G= NP_001269606.1:p.Leu812=
NM_001282678.1:c.1983G= NP_001269607.1:p.Leu661=
XM_005250433.3:c.858G= XP_005250490.1:p.Leu286=
XR_242246.3:n.2703G=
XM_017012319.2:c.858G= XP_016867808.1:p.Leu286=
XR_001744808.2:n.1634G=
XR_242246.5:n.2654G=
NM_000466.3:c.2607G= MANE Select NP_000457.1:p.Leu869=
NM_001282677.2:c.2436G= NP_001269606.1:p.Leu812=
NM_001282678.2:c.1983G= NP_001269607.1:p.Leu661=