Canonical Allele Identifier: CA1725936123
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92502002G= , CM000669.2:g.92502002G= GRCh38
NC_000007.13:g.92131316G= , CM000669.1:g.92131316G= GRCh37
NC_000007.12:g.91969252G= NCBI36
NG_008341.1:g.31530C=
NG_008341.2:g.31530C=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.2304C= MANE Select ENSP00000248633.4:p.Asp768=
ENST00000248633.8:c.2304C= ENSP00000248633.4:p.Asp768=
ENST00000428214.5:c.2133C= ENSP00000394413.1:p.Asp711=
ENST00000438045.5:c.1338C= ENSP00000410438.1:p.Asp446=
ENST00000484913.5:n.2343C=
ENST00000496092.1:n.102C=
ENST00000496420.5:n.1980C=
NM_000466.2:c.2304C= NP_000457.1:p.Asp768=
NM_001282677.1:c.2133C= NP_001269606.1:p.Asp711=
NM_001282678.1:c.1680C= NP_001269607.1:p.Asp560=
XM_005250433.3:c.555C= XP_005250490.1:p.Asp185=
XR_242246.3:n.2400C=
XM_017012319.2:c.555C= XP_016867808.1:p.Asp185=
XR_001744808.2:n.1331C=
XR_242246.5:n.2351C=
NM_000466.3:c.2304C= MANE Select NP_000457.1:p.Asp768=
NM_001282677.2:c.2133C= NP_001269606.1:p.Asp711=
NM_001282678.2:c.1680C= NP_001269607.1:p.Asp560=