Canonical Allele Identifier: CA456624094
Gene: PEX1 HGNC NCBI

Linked Data

dbSNP Id: rs1792863550
MyVariant Identifiers: chr7:g.92147031A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517717A>C , CM000669.2:g.92517717A>C GRCh38
NC_000007.13:g.92147031A>C , CM000669.1:g.92147031A>C GRCh37
NC_000007.12:g.91984967A>C NCBI36
NG_008341.1:g.15815T>G
NG_008341.2:g.15815T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000248633.9:c.798T>G MANE Select ENSP00000248633.4:p.Gly266=
ENST00000248633.8:c.798T>G ENSP00000248633.4:p.Gly266=
ENST00000428214.5:c.798T>G ENSP00000394413.1:p.Gly266=
ENST00000438045.5:c.274-3750T>G ENSP00000410438.1:n.274-3750T>G
ENST00000484913.5:n.837T>G
NM_000466.2:c.798T>G NP_000457.1:p.Gly266=
NM_001282677.1:c.798T>G NP_001269606.1:p.Gly266=
NM_001282678.1:c.174T>G NP_001269607.1:p.Gly58=
XR_242246.3:n.894T>G
XR_242246.5:n.845T>G
NM_000466.3:c.798T>G MANE Select NP_000457.1:p.Gly266=
NM_001282677.2:c.798T>G NP_001269606.1:p.Gly266=
NM_001282678.2:c.174T>G NP_001269607.1:p.Gly58=