Canonical Allele Identifier: CA246765
Gene: PEX26 HGNC NCBI

Linked Data

ClinVar Variation Id: 198225
dbSNP Id: rs794727805

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18087962T>G , CM000684.2:g.18087962T>G GRCh38
NC_000022.10:g.18570728T>G , CM000684.1:g.18570728T>G GRCh37
NC_000022.9:g.16950728T>G NCBI36
NG_008339.1:g.15043T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.815-10T>G MANE Select ENSP00000382648.4:n.815-10T>G
ENST00000474897.6:c.814+2704T>G ENSP00000434235.2:n.814+2704T>G
ENST00000329627.11:c.815-10T>G ENSP00000331106.5:n.815-10T>G
ENST00000399744.7:c.815-10T>G ENSP00000382648.3:n.815-10T>G
ENST00000428061.2:c.668-10T>G ENSP00000412441.2:n.668-10T>G
ENST00000474897.5:c.371+7948T>G ENSP00000434235.1:n.371+7948T>G
ENST00000610387.4:c.668-10T>G ENSP00000482091.1:n.668-10T>G
NM_001127649.2:c.815-10T>G NP_001121121.1:n.815-10T>G
NM_001199319.1:c.668-10T>G NP_001186248.1:n.668-10T>G
NM_017929.5:c.815-10T>G NP_060399.1:n.815-10T>G
NM_001127649.3:c.815-10T>G MANE Select NP_001121121.1:n.815-10T>G
NM_001199319.2:c.668-10T>G NP_001186248.1:n.668-10T>G
NM_017929.6:c.815-10T>G NP_060399.1:n.815-10T>G