Canonical Allele Identifier: CA2395402622

Gene: PEX26

Linked Data

• dbSNP Id: rs779022472

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078211_18078214dup , CM000684.2:g.18078211_18078214dup	GRCh38
NC_000022.10:g.18560977_18560980dup , CM000684.1:g.18560977_18560980dup	GRCh37
NC_000022.9:g.16940977_16940980dup	NCBI36
NG_008339.1:g.5292_5295dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-166_-163dup MANE Select	ENSP00000382648.4:n.-166_-163dup
ENST00000474897.6:c.-81-85_-81-82dup	ENSP00000434235.2:n.-81-85_-81-82dup
ENST00000329627.11:c.-81-85_-81-82dup	ENSP00000331106.5:n.-81-85_-81-82dup
ENST00000399744.7:c.-166_-163dup	ENSP00000382648.3:n.-166_-163dup
ENST00000474897.5:c.-166_-163dup	ENSP00000434235.1:n.-166_-163dup
ENST00000610387.4:c.-81-85_-81-82dup	ENSP00000482091.1:n.-81-85_-81-82dup
NM_001127649.2:c.-166_-163dup	NP_001121121.1:n.-166_-163dup
NM_001199319.1:c.-81-85_-81-82dup	NP_001186248.1:n.-81-85_-81-82dup
NM_017929.5:c.-81-85_-81-82dup	NP_060399.1:n.-81-85_-81-82dup
NM_001127649.3:c.-166_-163dup MANE Select	NP_001121121.1:n.-166_-163dup
NM_001199319.2:c.-81-85_-81-82dup	NP_001186248.1:n.-81-85_-81-82dup
NM_017929.6:c.-81-85_-81-82dup	NP_060399.1:n.-81-85_-81-82dup