Canonical Allele Identifier: CA2395402692

Gene: PEX26

Linked Data

• dbSNP Id: rs1795565050

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078343_18078345del , CM000684.2:g.18078343_18078345del	GRCh38
NC_000022.10:g.18561109_18561111del , CM000684.1:g.18561109_18561111del	GRCh37
NC_000022.9:g.16941109_16941111del	NCBI36
NG_008339.1:g.5424_5426del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-34_-32del MANE Select	ENSP00000382648.4:n.-34_-32del
ENST00000474897.6:c.-34_-32del	ENSP00000434235.2:n.-34_-32del
ENST00000329627.11:c.-34_-32del	ENSP00000331106.5:n.-34_-32del
ENST00000399744.7:c.-34_-32del	ENSP00000382648.3:n.-34_-32del
ENST00000474897.5:c.-34_-32del	ENSP00000434235.1:n.-34_-32del
ENST00000610387.4:c.-34_-32del	ENSP00000482091.1:n.-34_-32del
NM_001127649.2:c.-34_-32del	NP_001121121.1:n.-34_-32del
NM_001199319.1:c.-34_-32del	NP_001186248.1:n.-34_-32del
NM_017929.5:c.-34_-32del	NP_060399.1:n.-34_-32del
NM_001127649.3:c.-34_-32del MANE Select	NP_001121121.1:n.-34_-32del
NM_001199319.2:c.-34_-32del	NP_001186248.1:n.-34_-32del
NM_017929.6:c.-34_-32del	NP_060399.1:n.-34_-32del