Canonical Allele Identifier: CA456624346
Gene: PEX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92147283G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517969G>A , CM000669.2:g.92517969G>A GRCh38
NC_000007.13:g.92147283G>A , CM000669.1:g.92147283G>A GRCh37
NC_000007.12:g.91985219G>A NCBI36
NG_008341.1:g.15563C>T
NG_008341.2:g.15563C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.546C>T MANE Select ENSP00000248633.4:p.Arg182=
ENST00000248633.8:c.546C>T ENSP00000248633.4:p.Arg182=
ENST00000428214.5:c.546C>T ENSP00000394413.1:p.Arg182=
ENST00000438045.5:c.274-4002C>T ENSP00000410438.1:n.274-4002C>T
ENST00000484913.5:n.585C>T
NM_000466.2:c.546C>T NP_000457.1:p.Arg182=
NM_001282677.1:c.546C>T NP_001269606.1:p.Arg182=
NM_001282678.1:c.-79C>T NP_001269607.1:n.-79C>T
XR_242246.3:n.642C>T
XR_242246.5:n.593C>T
NM_000466.3:c.546C>T MANE Select NP_000457.1:p.Arg182=
NM_001282677.2:c.546C>T NP_001269606.1:p.Arg182=
NM_001282678.2:c.-79C>T NP_001269607.1:n.-79C>T