Canonical Allele Identifier: CA10093177
Gene: PEX26 HGNC NCBI

Linked Data

dbSNP Id: rs781474596

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.18078292C>T , CM000684.2:g.18078292C>T GRCh38
NC_000022.10:g.18561058C>T , CM000684.1:g.18561058C>T GRCh37
NC_000022.9:g.16941058C>T NCBI36
NG_008339.1:g.5373C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000399744.8:c.-85C>T MANE Select ENSP00000382648.4:n.-85C>T
ENST00000474897.6:c.-81-4C>T ENSP00000434235.2:n.-81-4C>T
ENST00000329627.11:c.-81-4C>T ENSP00000331106.5:n.-81-4C>T
ENST00000399744.7:c.-85C>T ENSP00000382648.3:n.-85C>T
ENST00000474897.5:c.-85C>T ENSP00000434235.1:n.-85C>T
ENST00000610387.4:c.-81-4C>T ENSP00000482091.1:n.-81-4C>T
NM_001127649.2:c.-85C>T NP_001121121.1:n.-85C>T
NM_001199319.1:c.-81-4C>T NP_001186248.1:n.-81-4C>T
NM_017929.5:c.-81-4C>T NP_060399.1:n.-81-4C>T
NM_001127649.3:c.-85C>T MANE Select NP_001121121.1:n.-85C>T
NM_001199319.2:c.-81-4C>T NP_001186248.1:n.-81-4C>T
NM_017929.6:c.-81-4C>T NP_060399.1:n.-81-4C>T