Canonical Allele Identifier: CA751300591

Gene: PEX26

Linked Data

• dbSNP Id: rs1355746278
• gnomAD v3: 22-18080063-T-A
• gnomAD v4: 22-18080063-T-A
• MyVariant Identifiers: chr22:g.18562829T>A (hg19) ; chr22:g.18080063T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18080063T>A , CM000684.2:g.18080063T>A	GRCh38
NC_000022.10:g.18562829T>A , CM000684.1:g.18562829T>A	GRCh37
NC_000022.9:g.16942829T>A	NCBI36
NG_008339.1:g.7144T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.371+49T>A MANE Select	ENSP00000382648.4:n.371+49T>A
ENST00000474897.6:c.371+49T>A	ENSP00000434235.2:n.371+49T>A
ENST00000329627.11:c.371+49T>A	ENSP00000331106.5:n.371+49T>A
ENST00000399744.7:c.371+49T>A	ENSP00000382648.3:n.371+49T>A
ENST00000428061.2:c.371+49T>A	ENSP00000412441.2:n.371+49T>A
ENST00000474897.5:c.371+49T>A	ENSP00000434235.1:n.371+49T>A
ENST00000610387.4:c.371+49T>A	ENSP00000482091.1:n.371+49T>A
NM_001127649.2:c.371+49T>A	NP_001121121.1:n.371+49T>A
NM_001199319.1:c.371+49T>A	NP_001186248.1:n.371+49T>A
NM_017929.5:c.371+49T>A	NP_060399.1:n.371+49T>A
NM_001127649.3:c.371+49T>A MANE Select	NP_001121121.1:n.371+49T>A
NM_001199319.2:c.371+49T>A	NP_001186248.1:n.371+49T>A
NM_017929.6:c.371+49T>A	NP_060399.1:n.371+49T>A