Canonical Allele Identifier: CA1725947141
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517275C= , CM000669.2:g.92517275C= GRCh38
NC_000007.13:g.92146589C= , CM000669.1:g.92146589C= GRCh37
NC_000007.12:g.91984525C= NCBI36
NG_008341.1:g.16257G=
NG_008341.2:g.16257G=

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.1239+1G= MANE Select ENSP00000248633.4:n.1239+1G=
ENST00000248633.8:c.1239+1G= ENSP00000248633.4:n.1239+1G=
ENST00000422866.1:c.140+1G=
ENST00000428214.5:c.1239+1G= ENSP00000394413.1:n.1239+1G=
ENST00000438045.5:c.274-3308G= ENSP00000410438.1:n.274-3308G=
ENST00000484913.5:n.1278+1G=
NM_000466.2:c.1239+1G= NP_000457.1:n.1239+1G=
NM_001282677.1:c.1239+1G= NP_001269606.1:n.1239+1G=
NM_001282678.1:c.615+1G= NP_001269607.1:n.615+1G=
XR_242246.3:n.1335+1G=
XM_017012319.2:c.-428+1G= XP_016867808.1:n.-428+1G=
XR_001744808.2:n.349+1G=
XR_242246.5:n.1286+1G=
NM_000466.3:c.1239+1G= MANE Select NP_000457.1:n.1239+1G=
NM_001282677.2:c.1239+1G= NP_001269606.1:n.1239+1G=
NM_001282678.2:c.615+1G= NP_001269607.1:n.615+1G=