Canonical Allele Identifier: CA10093242
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 287773
dbSNP Id: rs374290931

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078574C>T , CM000684.2:g.18078574C>T GRCh38
NC_000022.10:g.18561340C>T , CM000684.1:g.18561340C>T GRCh37
NC_000022.9:g.16941340C>T NCBI36
NG_008339.1:g.5655C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.198C>T MANE Select ENSP00000382648.4:p.Ala66=
ENST00000474897.6:c.198C>T ENSP00000434235.2:p.Ala66=
ENST00000329627.11:c.198C>T ENSP00000331106.5:p.Ala66=
ENST00000399744.7:c.198C>T ENSP00000382648.3:p.Ala66=
ENST00000428061.2:c.198C>T ENSP00000412441.2:p.Ala66=
ENST00000474897.5:c.198C>T ENSP00000434235.1:p.Ala66=
ENST00000610387.4:c.198C>T ENSP00000482091.1:p.Ala66=
NM_001127649.2:c.198C>T NP_001121121.1:p.Ala66=
NM_001199319.1:c.198C>T NP_001186248.1:p.Ala66=
NM_017929.5:c.198C>T NP_060399.1:p.Ala66=
NM_001127649.3:c.198C>T MANE Select NP_001121121.1:p.Ala66=
NM_001199319.2:c.198C>T NP_001186248.1:p.Ala66=
NM_017929.6:c.198C>T NP_060399.1:p.Ala66=