Canonical Allele Identifier: CA1725948310
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92518045G= , CM000669.2:g.92518045G= GRCh38
NC_000007.13:g.92147359G= , CM000669.1:g.92147359G= GRCh37
NC_000007.12:g.91985295G= NCBI36
NG_008341.1:g.15487C=
NG_008341.2:g.15487C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.473-3C= MANE Select ENSP00000248633.4:n.473-3C=
ENST00000248633.8:c.473-3C= ENSP00000248633.4:n.473-3C=
ENST00000428214.5:c.473-3C= ENSP00000394413.1:n.473-3C=
ENST00000438045.5:c.273+4057C= ENSP00000410438.1:n.273+4057C=
ENST00000484913.5:n.512-3C=
NM_000466.2:c.473-3C= NP_000457.1:n.473-3C=
NM_001282677.1:c.473-3C= NP_001269606.1:n.473-3C=
NM_001282678.1:c.-152-3C= NP_001269607.1:n.-152-3C=
XR_242246.3:n.569-3C=
XR_242246.5:n.520-3C=
NM_000466.3:c.473-3C= MANE Select NP_000457.1:n.473-3C=
NM_001282677.2:c.473-3C= NP_001269606.1:n.473-3C=
NM_001282678.2:c.-152-3C= NP_001269607.1:n.-152-3C=