Canonical Allele Identifier: CA2655183124

Gene: PEX26

Linked Data

• gnomAD v4: 22-18078288-T-TCGC

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078290_18078292dup , CM000684.2:g.18078290_18078292dup	GRCh38
NC_000022.10:g.18561056_18561058dup , CM000684.1:g.18561056_18561058dup	GRCh37
NC_000022.9:g.16941056_16941058dup	NCBI36
NG_008339.1:g.5371_5373dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-87_-85dup MANE Select	ENSP00000382648.4:n.-87_-85dup
ENST00000474897.6:c.-81-6_-81-4dup	ENSP00000434235.2:n.-81-6_-81-4dup
ENST00000329627.11:c.-81-6_-81-4dup	ENSP00000331106.5:n.-81-6_-81-4dup
ENST00000399744.7:c.-87_-85dup	ENSP00000382648.3:n.-87_-85dup
ENST00000474897.5:c.-87_-85dup	ENSP00000434235.1:n.-87_-85dup
ENST00000610387.4:c.-81-6_-81-4dup	ENSP00000482091.1:n.-81-6_-81-4dup
NM_001127649.2:c.-87_-85dup	NP_001121121.1:n.-87_-85dup
NM_001199319.1:c.-81-6_-81-4dup	NP_001186248.1:n.-81-6_-81-4dup
NM_017929.5:c.-81-6_-81-4dup	NP_060399.1:n.-81-6_-81-4dup
NM_001127649.3:c.-87_-85dup MANE Select	NP_001121121.1:n.-87_-85dup
NM_001199319.2:c.-81-6_-81-4dup	NP_001186248.1:n.-81-6_-81-4dup
NM_017929.6:c.-81-6_-81-4dup	NP_060399.1:n.-81-6_-81-4dup