Canonical Allele Identifier: CA2395402900
Gene: PEX26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078698_18078699delinsCA , CM000684.2:g.18078698_18078699delinsCA GRCh38
NC_000022.10:g.18561464_18561465delinsCA , CM000684.1:g.18561464_18561465delinsCA GRCh37
NC_000022.9:g.16941464_16941465delinsCA NCBI36
NG_008339.1:g.5779_5780delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.230+92_230+93delinsCA MANE Select ENSP00000382648.4:n.230+92_230+93delinsCA
ENST00000474897.6:c.230+92_230+93delinsCA ENSP00000434235.2:n.230+92_230+93delinsCA
ENST00000329627.11:c.230+92_230+93delinsCA ENSP00000331106.5:n.230+92_230+93delinsCA
ENST00000399744.7:c.230+92_230+93delinsCA ENSP00000382648.3:n.230+92_230+93delinsCA
ENST00000428061.2:c.230+92_230+93delinsCA ENSP00000412441.2:n.230+92_230+93delinsCA
ENST00000474897.5:c.230+92_230+93delinsCA ENSP00000434235.1:n.230+92_230+93delinsCA
ENST00000610387.4:c.230+92_230+93delinsCA ENSP00000482091.1:n.230+92_230+93delinsCA
NM_001127649.2:c.230+92_230+93delinsCA NP_001121121.1:n.230+92_230+93delinsCA
NM_001199319.1:c.230+92_230+93delinsCA NP_001186248.1:n.230+92_230+93delinsCA
NM_017929.5:c.230+92_230+93delinsCA NP_060399.1:n.230+92_230+93delinsCA
NM_001127649.3:c.230+92_230+93delinsCA MANE Select NP_001121121.1:n.230+92_230+93delinsCA
NM_001199319.2:c.230+92_230+93delinsCA NP_001186248.1:n.230+92_230+93delinsCA
NM_017929.6:c.230+92_230+93delinsCA NP_060399.1:n.230+92_230+93delinsCA