Canonical Allele Identifier: CA410264690

Gene: PEX26

Linked Data

• ClinVar Variation Id: 2065411
• ClinVar RCV Id: RCV002958453
• MyVariant Identifiers: chr22:g.18561263G>A (hg19) ; chr22:g.18078497G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078497G>A , CM000684.2:g.18078497G>A	GRCh38
NC_000022.10:g.18561263G>A , CM000684.1:g.18561263G>A	GRCh37
NC_000022.9:g.16941263G>A	NCBI36
NG_008339.1:g.5578G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.121G>A MANE Select	ENSP00000382648.4:p.Ala41Thr
ENST00000474897.6:c.121G>A	ENSP00000434235.2:p.Ala41Thr
ENST00000329627.11:c.121G>A	ENSP00000331106.5:p.Ala41Thr
ENST00000399744.7:c.121G>A	ENSP00000382648.3:p.Ala41Thr
ENST00000428061.2:c.121G>A	ENSP00000412441.2:p.Ala41Thr
ENST00000474897.5:c.121G>A	ENSP00000434235.1:p.Ala41Thr
ENST00000610387.4:c.121G>A	ENSP00000482091.1:p.Ala41Thr
NM_001127649.2:c.121G>A	NP_001121121.1:p.Ala41Thr
NM_001199319.1:c.121G>A	NP_001186248.1:p.Ala41Thr
NM_017929.5:c.121G>A	NP_060399.1:p.Ala41Thr
NM_001127649.3:c.121G>A MANE Select	NP_001121121.1:p.Ala41Thr
NM_001199319.2:c.121G>A	NP_001186248.1:p.Ala41Thr
NM_017929.6:c.121G>A	NP_060399.1:p.Ala41Thr