Canonical Allele Identifier: CA456624406
Gene: PEX1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr7:g.92147301A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.92517987A>G , CM000669.2:g.92517987A>G GRCh38
NC_000007.13:g.92147301A>G , CM000669.1:g.92147301A>G GRCh37
NC_000007.12:g.91985237A>G NCBI36
NG_008341.1:g.15545T>C
NG_008341.2:g.15545T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248633.9:c.528T>C MANE Select ENSP00000248633.4:p.Leu176=
ENST00000248633.8:c.528T>C ENSP00000248633.4:p.Leu176=
ENST00000428214.5:c.528T>C ENSP00000394413.1:p.Leu176=
ENST00000438045.5:c.274-4020T>C ENSP00000410438.1:n.274-4020T>C
ENST00000484913.5:n.567T>C
NM_000466.2:c.528T>C NP_000457.1:p.Leu176=
NM_001282677.1:c.528T>C NP_001269606.1:p.Leu176=
NM_001282678.1:c.-97T>C NP_001269607.1:n.-97T>C
XR_242246.3:n.624T>C
XR_242246.5:n.575T>C
NM_000466.3:c.528T>C MANE Select NP_000457.1:p.Leu176=
NM_001282677.2:c.528T>C NP_001269606.1:p.Leu176=
NM_001282678.2:c.-97T>C NP_001269607.1:n.-97T>C