Canonical Allele Identifier: CA1024000648

Gene: PEX26

Linked Data

• gnomAD v3: 22-18080053-A-AGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT
• gnomAD v4: 22-18080053-A-AGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18080053_18080054insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT , CM000684.2:g.18080053_18080054insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	GRCh38
NC_000022.10:g.18562819_18562820insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT , CM000684.1:g.18562819_18562820insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	GRCh37
NC_000022.9:g.16942819_16942820insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	NCBI36
NG_008339.1:g.7134_7135insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT MANE Select	ENSP00000382648.4:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGC...
ENST00000474897.6:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	ENSP00000434235.2:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGC...
ENST00000329627.11:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	ENSP00000331106.5:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGC...
ENST00000399744.7:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	ENSP00000382648.3:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGC...
ENST00000428061.2:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	ENSP00000412441.2:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGC...
ENST00000474897.5:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	ENSP00000434235.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGC...
ENST00000610387.4:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	ENSP00000482091.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGC...
NM_001127649.2:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	NP_001121121.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCAC...
NM_001199319.1:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	NP_001186248.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCAC...
NM_017929.5:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	NP_060399.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAG...
NM_001127649.3:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT MANE Select	NP_001121121.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCAC...
NM_001199319.2:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	NP_001186248.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCAC...
NM_017929.6:c.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAGCCT	NP_060399.1:n.371+39_371+40insGGGCTTGCATTGCTCTTTCTAATGCCACCAG...