Canonical Allele Identifier: CA2655183317

Gene: PEX26

Linked Data

• gnomAD v4: 22-18078345-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078346dup , CM000684.2:g.18078346dup	GRCh38
NC_000022.10:g.18561112dup , CM000684.1:g.18561112dup	GRCh37
NC_000022.9:g.16941112dup	NCBI36
NG_008339.1:g.5427dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-31dup MANE Select	ENSP00000382648.4:n.-31dup
ENST00000474897.6:c.-31dup	ENSP00000434235.2:n.-31dup
ENST00000329627.11:c.-31dup	ENSP00000331106.5:n.-31dup
ENST00000399744.7:c.-31dup	ENSP00000382648.3:n.-31dup
ENST00000474897.5:c.-31dup	ENSP00000434235.1:n.-31dup
ENST00000610387.4:c.-31dup	ENSP00000482091.1:n.-31dup
NM_001127649.2:c.-31dup	NP_001121121.1:n.-31dup
NM_001199319.1:c.-31dup	NP_001186248.1:n.-31dup
NM_017929.5:c.-31dup	NP_060399.1:n.-31dup
NM_001127649.3:c.-31dup MANE Select	NP_001121121.1:n.-31dup
NM_001199319.2:c.-31dup	NP_001186248.1:n.-31dup
NM_017929.6:c.-31dup	NP_060399.1:n.-31dup