Canonical Allele Identifier: CA10093224
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 2169751
ClinVar RCV Id: RCV003093244
dbSNP Id: rs757375227

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078479G>A , CM000684.2:g.18078479G>A GRCh38
NC_000022.10:g.18561245G>A , CM000684.1:g.18561245G>A GRCh37
NC_000022.9:g.16941245G>A NCBI36
NG_008339.1:g.5560G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.103G>A MANE Select ENSP00000382648.4:p.Val35Met
ENST00000474897.6:c.103G>A ENSP00000434235.2:p.Val35Met
ENST00000329627.11:c.103G>A ENSP00000331106.5:p.Val35Met
ENST00000399744.7:c.103G>A ENSP00000382648.3:p.Val35Met
ENST00000428061.2:c.103G>A ENSP00000412441.2:p.Val35Met
ENST00000474897.5:c.103G>A ENSP00000434235.1:p.Val35Met
ENST00000610387.4:c.103G>A ENSP00000482091.1:p.Val35Met
NM_001127649.2:c.103G>A NP_001121121.1:p.Val35Met
NM_001199319.1:c.103G>A NP_001186248.1:p.Val35Met
NM_017929.5:c.103G>A NP_060399.1:p.Val35Met
NM_001127649.3:c.103G>A MANE Select NP_001121121.1:p.Val35Met
NM_001199319.2:c.103G>A NP_001186248.1:p.Val35Met
NM_017929.6:c.103G>A NP_060399.1:p.Val35Met