Canonical Allele Identifier: CA1725947717
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517684C= , CM000669.2:g.92517684C= GRCh38
NC_000007.13:g.92146998C= , CM000669.1:g.92146998C= GRCh37
NC_000007.12:g.91984934C= NCBI36
NG_008341.1:g.15848G=
NG_008341.2:g.15848G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.831G= MANE Select ENSP00000248633.4:p.Gln277=
ENST00000248633.8:c.831G= ENSP00000248633.4:p.Gln277=
ENST00000428214.5:c.831G= ENSP00000394413.1:p.Gln277=
ENST00000438045.5:c.274-3717G= ENSP00000410438.1:n.274-3717G=
ENST00000484913.5:n.870G=
NM_000466.2:c.831G= NP_000457.1:p.Gln277=
NM_001282677.1:c.831G= NP_001269606.1:p.Gln277=
NM_001282678.1:c.207G= NP_001269607.1:p.Gln69=
XR_242246.3:n.927G=
XR_242246.5:n.878G=
NM_000466.3:c.831G= MANE Select NP_000457.1:p.Gln277=
NM_001282677.2:c.831G= NP_001269606.1:p.Gln277=
NM_001282678.2:c.207G= NP_001269607.1:p.Gln69=