Canonical Allele Identifier: CA2740094766

Gene: PEX26

Linked Data

• ClinVar Variation Id: 2934975
• ClinVar RCV Id: RCV003798677

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078374_18078393delinsTGCAGCCCCCCTCAGGGGGCTCGGGG , CM000684.2:g.18078374_18078393delinsTGCAGCCCCCCTCAGGGGGCTCGGGG	GRCh38
NC_000022.10:g.18561140_18561159delinsTGCAGCCCCCCTCAGGGGGCTCGGGG , CM000684.1:g.18561140_18561159delinsTGCAGCCCCCCTCAGGGGGCTCGGGG	GRCh37
NC_000022.9:g.16941140_16941159delinsTGCAGCCCCCCTCAGGGGGCTCGGGG	NCBI36
NG_008339.1:g.5455_5474delinsTGCAGCCCCCCTCAGGGGGCTCGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
ENST00000474897.6:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
ENST00000329627.11:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
ENST00000399744.7:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
ENST00000474897.5:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
ENST00000610387.4:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
NM_001127649.2:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
NM_001199319.1:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
NM_017929.5:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
NM_001127649.3:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
NM_001199319.2:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG
NM_017929.6:c.-3_17delinsTGCAGCCCCCCTCAGGGGGCTCGGGG