Canonical Allele Identifier: CA456484074
Gene: PEX1 HGNC NCBI

Linked Data

gnomAD v4: 7-92522120-T-A
MyVariant Identifiers: chr7:g.92151434T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522120T>A , CM000669.2:g.92522120T>A GRCh38
NC_000007.13:g.92151434T>A , CM000669.1:g.92151434T>A GRCh37
NC_000007.12:g.91989370T>A NCBI36
NG_008341.1:g.11412A>T
NG_008341.2:g.11412A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.255A>T MANE Select ENSP00000248633.4:p.Gly85=
ENST00000248633.8:c.255A>T ENSP00000248633.4:p.Gly85=
ENST00000428214.5:c.255A>T ENSP00000394413.1:p.Gly85=
ENST00000438045.5:c.255A>T ENSP00000410438.1:p.Gly85=
ENST00000484913.5:n.259A>T
NM_000466.2:c.255A>T NP_000457.1:p.Gly85=
NM_001282677.1:c.255A>T NP_001269606.1:p.Gly85=
NM_001282678.1:c.-405A>T NP_001269607.1:n.-405A>T
XR_242246.3:n.351A>T
XR_242246.5:n.302A>T
NM_000466.3:c.255A>T MANE Select NP_000457.1:p.Gly85=
NM_001282677.2:c.255A>T NP_001269606.1:p.Gly85=
NM_001282678.2:c.-405A>T NP_001269607.1:n.-405A>T