Canonical Allele Identifier: CA456484129
Gene: PEX1 HGNC NCBI

Linked Data

gnomAD v4: 7-92522225-G-A
MyVariant Identifiers: chr7:g.92151539G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92522225G>A , CM000669.2:g.92522225G>A GRCh38
NC_000007.13:g.92151539G>A , CM000669.1:g.92151539G>A GRCh37
NC_000007.12:g.91989475G>A NCBI36
NG_008341.1:g.11307C>T
NG_008341.2:g.11307C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.150C>T MANE Select ENSP00000248633.4:p.Val50=
ENST00000248633.8:c.150C>T ENSP00000248633.4:p.Val50=
ENST00000428214.5:c.150C>T ENSP00000394413.1:p.Val50=
ENST00000438045.5:c.150C>T ENSP00000410438.1:p.Val50=
ENST00000484913.5:n.154C>T
NM_000466.2:c.150C>T NP_000457.1:p.Val50=
NM_001282677.1:c.150C>T NP_001269606.1:p.Val50=
NM_001282678.1:c.-510C>T NP_001269607.1:n.-510C>T
XR_242246.3:n.246C>T
XR_242246.5:n.197C>T
NM_000466.3:c.150C>T MANE Select NP_000457.1:p.Val50=
NM_001282677.2:c.150C>T NP_001269606.1:p.Val50=
NM_001282678.2:c.-510C>T NP_001269607.1:n.-510C>T