Canonical Allele Identifier: CA1725946732
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92510849T= , CM000669.2:g.92510849T= GRCh38
NC_000007.13:g.92140163T= , CM000669.1:g.92140163T= GRCh37
NC_000007.12:g.91978099T= NCBI36
NG_008341.1:g.22683A=
NG_008341.2:g.22683A=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.1587+95A= MANE Select ENSP00000248633.4:n.1587+95A=
ENST00000248633.8:c.1587+95A= ENSP00000248633.4:n.1587+95A=
ENST00000422866.1:c.488+95A=
ENST00000428214.5:c.1587+95A= ENSP00000394413.1:n.1587+95A=
ENST00000438045.5:c.621+95A= ENSP00000410438.1:n.621+95A=
ENST00000484913.5:n.1626+95A=
NM_000466.2:c.1587+95A= NP_000457.1:n.1587+95A=
NM_001282677.1:c.1587+95A= NP_001269606.1:n.1587+95A=
NM_001282678.1:c.963+95A= NP_001269607.1:n.963+95A=
XM_005250433.3:c.-80+95A= XP_005250490.1:n.-80+95A=
XR_242246.3:n.1683+95A=
XM_017012319.2:c.-80+95A= XP_016867808.1:n.-80+95A=
XR_001744808.2:n.697+95A=
XR_242246.5:n.1634+95A=
NM_000466.3:c.1587+95A= MANE Select NP_000457.1:n.1587+95A=
NM_001282677.2:c.1587+95A= NP_001269606.1:n.1587+95A=
NM_001282678.2:c.963+95A= NP_001269607.1:n.963+95A=