Canonical Allele Identifier: CA2655184201

Gene: PEX26

Linked Data

• gnomAD v4: 22-18078572-G-GCCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078576_18078579dup , CM000684.2:g.18078576_18078579dup	GRCh38
NC_000022.10:g.18561342_18561345dup , CM000684.1:g.18561342_18561345dup	GRCh37
NC_000022.9:g.16941342_16941345dup	NCBI36
NG_008339.1:g.5657_5660dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.200_203dup MANE Select	ENSP00000382648.4:p.His68GlnfsTer?
ENST00000474897.6:c.200_203dup	ENSP00000434235.2:p.His68GlnfsTer?
ENST00000329627.11:c.200_203dup	ENSP00000331106.5:p.His68GlnfsTer?
ENST00000399744.7:c.200_203dup	ENSP00000382648.3:p.His68GlnfsTer?
ENST00000428061.2:c.200_203dup	ENSP00000412441.2:p.His68GlnfsTer?
ENST00000474897.5:c.200_203dup	ENSP00000434235.1:p.His68GlnfsTer?
ENST00000610387.4:c.200_203dup	ENSP00000482091.1:p.His68GlnfsTer?
NM_001127649.2:c.200_203dup	NP_001121121.1:p.His68GlnfsTer?
NM_001199319.1:c.200_203dup	NP_001186248.1:p.His68GlnfsTer?
NM_017929.5:c.200_203dup	NP_060399.1:p.His68GlnfsTer?
NM_001127649.3:c.200_203dup MANE Select	NP_001121121.1:p.His68GlnfsTer?
NM_001199319.2:c.200_203dup	NP_001186248.1:p.His68GlnfsTer?
NM_017929.6:c.200_203dup	NP_060399.1:p.His68GlnfsTer?