Canonical Allele Identifier: CA10093167

Gene: PEX26

Linked Data

• dbSNP Id: rs779022472
• ExAC: 22:18560974 CAGAT / C
• gnomAD v2: 22-18560974-CAGAT-C
• gnomAD v3: 22-18078208-CAGAT-C
• gnomAD v4: 22-18078208-CAGAT-C
• MyVariant Identifiers: chr22:g.18560975_18560978del (hg19) ; chr22:g.18078209_18078212del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078211_18078214del , CM000684.2:g.18078211_18078214del	GRCh38
NC_000022.10:g.18560977_18560980del , CM000684.1:g.18560977_18560980del	GRCh37
NC_000022.9:g.16940977_16940980del	NCBI36
NG_008339.1:g.5292_5295del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-166_-163del MANE Select	ENSP00000382648.4:n.-166_-163del
ENST00000474897.6:c.-81-85_-81-82del	ENSP00000434235.2:n.-81-85_-81-82del
ENST00000329627.11:c.-81-85_-81-82del	ENSP00000331106.5:n.-81-85_-81-82del
ENST00000399744.7:c.-166_-163del	ENSP00000382648.3:n.-166_-163del
ENST00000474897.5:c.-166_-163del	ENSP00000434235.1:n.-166_-163del
ENST00000610387.4:c.-81-85_-81-82del	ENSP00000482091.1:n.-81-85_-81-82del
NM_001127649.2:c.-166_-163del	NP_001121121.1:n.-166_-163del
NM_001199319.1:c.-81-85_-81-82del	NP_001186248.1:n.-81-85_-81-82del
NM_017929.5:c.-81-85_-81-82del	NP_060399.1:n.-81-85_-81-82del
NM_001127649.3:c.-166_-163del MANE Select	NP_001121121.1:n.-166_-163del
NM_001199319.2:c.-81-85_-81-82del	NP_001186248.1:n.-81-85_-81-82del
NM_017929.6:c.-81-85_-81-82del	NP_060399.1:n.-81-85_-81-82del