Canonical Allele Identifier: CA2395402681
Gene: PEX26 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078332_18078336delinsGTCAC , CM000684.2:g.18078332_18078336delinsGTCAC GRCh38
NC_000022.10:g.18561098_18561102delinsGTCAC , CM000684.1:g.18561098_18561102delinsGTCAC GRCh37
NC_000022.9:g.16941098_16941102delinsGTCAC NCBI36
NG_008339.1:g.5413_5417delinsGTCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.-45_-41delinsGTCAC MANE Select ENSP00000382648.4:n.-45_-41delinsGTCAC
ENST00000474897.6:c.-45_-41delinsGTCAC ENSP00000434235.2:n.-45_-41delinsGTCAC
ENST00000329627.11:c.-45_-41delinsGTCAC ENSP00000331106.5:n.-45_-41delinsGTCAC
ENST00000399744.7:c.-45_-41delinsGTCAC ENSP00000382648.3:n.-45_-41delinsGTCAC
ENST00000474897.5:c.-45_-41delinsGTCAC ENSP00000434235.1:n.-45_-41delinsGTCAC
ENST00000610387.4:c.-45_-41delinsGTCAC ENSP00000482091.1:n.-45_-41delinsGTCAC
NM_001127649.2:c.-45_-41delinsGTCAC NP_001121121.1:n.-45_-41delinsGTCAC
NM_001199319.1:c.-45_-41delinsGTCAC NP_001186248.1:n.-45_-41delinsGTCAC
NM_017929.5:c.-45_-41delinsGTCAC NP_060399.1:n.-45_-41delinsGTCAC
NM_001127649.3:c.-45_-41delinsGTCAC MANE Select NP_001121121.1:n.-45_-41delinsGTCAC
NM_001199319.2:c.-45_-41delinsGTCAC NP_001186248.1:n.-45_-41delinsGTCAC
NM_017929.6:c.-45_-41delinsGTCAC NP_060399.1:n.-45_-41delinsGTCAC