Canonical Allele Identifier: CA1024000681

Gene: PEX26

Linked Data

• dbSNP Id: rs1926496059
• gnomAD v3: 22-18080124-G-A
• gnomAD v4: 22-18080124-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18080124G>A , CM000684.2:g.18080124G>A	GRCh38
NC_000022.10:g.18562890G>A , CM000684.1:g.18562890G>A	GRCh37
NC_000022.9:g.16942890G>A	NCBI36
NG_008339.1:g.7205G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.371+110G>A MANE Select	ENSP00000382648.4:n.371+110G>A
ENST00000474897.6:c.371+110G>A	ENSP00000434235.2:n.371+110G>A
ENST00000329627.11:c.371+110G>A	ENSP00000331106.5:n.371+110G>A
ENST00000399744.7:c.371+110G>A	ENSP00000382648.3:n.371+110G>A
ENST00000428061.2:c.371+110G>A	ENSP00000412441.2:n.371+110G>A
ENST00000474897.5:c.371+110G>A	ENSP00000434235.1:n.371+110G>A
ENST00000610387.4:c.371+110G>A	ENSP00000482091.1:n.371+110G>A
NM_001127649.2:c.371+110G>A	NP_001121121.1:n.371+110G>A
NM_001199319.1:c.371+110G>A	NP_001186248.1:n.371+110G>A
NM_017929.5:c.371+110G>A	NP_060399.1:n.371+110G>A
NM_001127649.3:c.371+110G>A MANE Select	NP_001121121.1:n.371+110G>A
NM_001199319.2:c.371+110G>A	NP_001186248.1:n.371+110G>A
NM_017929.6:c.371+110G>A	NP_060399.1:n.371+110G>A