Canonical Allele Identifier: CA2655186123

Gene: PEX26

Linked Data

• gnomAD v4: 22-18079749-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18079749C>G , CM000684.2:g.18079749C>G	GRCh38
NC_000022.10:g.18562515C>G , CM000684.1:g.18562515C>G	GRCh37
NC_000022.9:g.16942515C>G	NCBI36
NG_008339.1:g.6830C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000399744.8:c.231-125C>G MANE Select	ENSP00000382648.4:n.231-125C>G
ENST00000474897.6:c.231-125C>G	ENSP00000434235.2:n.231-125C>G
ENST00000329627.11:c.231-125C>G	ENSP00000331106.5:n.231-125C>G
ENST00000399744.7:c.231-125C>G	ENSP00000382648.3:n.231-125C>G
ENST00000428061.2:c.231-125C>G	ENSP00000412441.2:n.231-125C>G
ENST00000474897.5:c.231-125C>G	ENSP00000434235.1:n.231-125C>G
ENST00000610387.4:c.231-125C>G	ENSP00000482091.1:n.231-125C>G
NM_001127649.2:c.231-125C>G	NP_001121121.1:n.231-125C>G
NM_001199319.1:c.231-125C>G	NP_001186248.1:n.231-125C>G
NM_017929.5:c.231-125C>G	NP_060399.1:n.231-125C>G
NM_001127649.3:c.231-125C>G MANE Select	NP_001121121.1:n.231-125C>G
NM_001199319.2:c.231-125C>G	NP_001186248.1:n.231-125C>G
NM_017929.6:c.231-125C>G	NP_060399.1:n.231-125C>G