Canonical Allele Identifier: CA1725948226
Gene: PEX1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517982T= , CM000669.2:g.92517982T= GRCh38
NC_000007.13:g.92147296T= , CM000669.1:g.92147296T= GRCh37
NC_000007.12:g.91985232T= NCBI36
NG_008341.1:g.15550A=
NG_008341.2:g.15550A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.533A= MANE Select ENSP00000248633.4:p.Gln178=
ENST00000248633.8:c.533A= ENSP00000248633.4:p.Gln178=
ENST00000428214.5:c.533A= ENSP00000394413.1:p.Gln178=
ENST00000438045.5:c.274-4015A= ENSP00000410438.1:n.274-4015A=
ENST00000484913.5:n.572A=
NM_000466.2:c.533A= NP_000457.1:p.Gln178=
NM_001282677.1:c.533A= NP_001269606.1:p.Gln178=
NM_001282678.1:c.-92A= NP_001269607.1:n.-92A=
XR_242246.3:n.629A=
XR_242246.5:n.580A=
NM_000466.3:c.533A= MANE Select NP_000457.1:p.Gln178=
NM_001282677.2:c.533A= NP_001269606.1:p.Gln178=
NM_001282678.2:c.-92A= NP_001269607.1:n.-92A=