Canonical Allele Identifier: CA1725947425
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517504C= , CM000669.2:g.92517504C= GRCh38
NC_000007.13:g.92146818C= , CM000669.1:g.92146818C= GRCh37
NC_000007.12:g.91984754C= NCBI36
NG_008341.1:g.16028G=
NG_008341.2:g.16028G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.1011G= MANE Select ENSP00000248633.4:p.Lys337=
ENST00000248633.8:c.1011G= ENSP00000248633.4:p.Lys337=
ENST00000428214.5:c.1011G= ENSP00000394413.1:p.Lys337=
ENST00000438045.5:c.274-3537G= ENSP00000410438.1:n.274-3537G=
ENST00000484913.5:n.1050G=
NM_000466.2:c.1011G= NP_000457.1:p.Lys337=
NM_001282677.1:c.1011G= NP_001269606.1:p.Lys337=
NM_001282678.1:c.387G= NP_001269607.1:p.Lys129=
XR_242246.3:n.1107G=
XM_017012319.2:c.-656G= XP_016867808.1:n.-656G=
XR_001744808.2:n.121G=
XR_242246.5:n.1058G=
NM_000466.3:c.1011G= MANE Select NP_000457.1:p.Lys337=
NM_001282677.2:c.1011G= NP_001269606.1:p.Lys337=
NM_001282678.2:c.387G= NP_001269607.1:p.Lys129=