Canonical Allele Identifier: CA410264690
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2065411
ClinVar RCV Id: RCV002958453

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078497G>A , CM000684.2:g.18078497G>A GRCh38
NC_000022.10:g.18561263G>A , CM000684.1:g.18561263G>A GRCh37
NC_000022.9:g.16941263G>A NCBI36
NG_008339.1:g.5578G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.121G>A MANE Select ENSP00000382648.4:p.Ala41Thr
ENST00000474897.6:c.121G>A ENSP00000434235.2:p.Ala41Thr
ENST00000329627.11:c.121G>A ENSP00000331106.5:p.Ala41Thr
ENST00000399744.7:c.121G>A ENSP00000382648.3:p.Ala41Thr
ENST00000428061.2:c.121G>A ENSP00000412441.2:p.Ala41Thr
ENST00000474897.5:c.121G>A ENSP00000434235.1:p.Ala41Thr
ENST00000610387.4:c.121G>A ENSP00000482091.1:p.Ala41Thr
NM_001127649.2:c.121G>A NP_001121121.1:p.Ala41Thr
NM_001199319.1:c.121G>A NP_001186248.1:p.Ala41Thr
NM_017929.5:c.121G>A NP_060399.1:p.Ala41Thr
NM_001127649.3:c.121G>A MANE Select NP_001121121.1:p.Ala41Thr
NM_001199319.2:c.121G>A NP_001186248.1:p.Ala41Thr
NM_017929.6:c.121G>A NP_060399.1:p.Ala41Thr