Canonical Allele Identifier: CA1725951660
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522170G= , CM000669.2:g.92522170G= GRCh38
NC_000007.13:g.92151484G= , CM000669.1:g.92151484G= GRCh37
NC_000007.12:g.91989420G= NCBI36
NG_008341.1:g.11362C=
NG_008341.2:g.11362C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.205C= MANE Select ENSP00000248633.4:p.Gln69=
ENST00000248633.8:c.205C= ENSP00000248633.4:p.Gln69=
ENST00000428214.5:c.205C= ENSP00000394413.1:p.Gln69=
ENST00000438045.5:c.205C= ENSP00000410438.1:p.Gln69=
ENST00000484913.5:n.209C=
NM_000466.2:c.205C= NP_000457.1:p.Gln69=
NM_001282677.1:c.205C= NP_001269606.1:p.Gln69=
NM_001282678.1:c.-455C= NP_001269607.1:n.-455C=
XR_242246.3:n.301C=
XR_242246.5:n.252C=
NM_000466.3:c.205C= MANE Select NP_000457.1:p.Gln69=
NM_001282677.2:c.205C= NP_001269606.1:p.Gln69=
NM_001282678.2:c.-455C= NP_001269607.1:n.-455C=