Canonical Allele Identifier: CA2655186133

Gene: PEX26

Linked Data

• gnomAD v4: 22-18079753-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18079754_18079755del , CM000684.2:g.18079754_18079755del	GRCh38
NC_000022.10:g.18562520_18562521del , CM000684.1:g.18562520_18562521del	GRCh37
NC_000022.9:g.16942520_16942521del	NCBI36
NG_008339.1:g.6835_6836del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.231-120_231-119del MANE Select	ENSP00000382648.4:n.231-120_231-119del
ENST00000474897.6:c.231-120_231-119del	ENSP00000434235.2:n.231-120_231-119del
ENST00000329627.11:c.231-120_231-119del	ENSP00000331106.5:n.231-120_231-119del
ENST00000399744.7:c.231-120_231-119del	ENSP00000382648.3:n.231-120_231-119del
ENST00000428061.2:c.231-120_231-119del	ENSP00000412441.2:n.231-120_231-119del
ENST00000474897.5:c.231-120_231-119del	ENSP00000434235.1:n.231-120_231-119del
ENST00000610387.4:c.231-120_231-119del	ENSP00000482091.1:n.231-120_231-119del
NM_001127649.2:c.231-120_231-119del	NP_001121121.1:n.231-120_231-119del
NM_001199319.1:c.231-120_231-119del	NP_001186248.1:n.231-120_231-119del
NM_017929.5:c.231-120_231-119del	NP_060399.1:n.231-120_231-119del
NM_001127649.3:c.231-120_231-119del MANE Select	NP_001121121.1:n.231-120_231-119del
NM_001199319.2:c.231-120_231-119del	NP_001186248.1:n.231-120_231-119del
NM_017929.6:c.231-120_231-119del	NP_060399.1:n.231-120_231-119del