Canonical Allele Identifier: CA2395402652

Gene: PEX26

Linked Data

• dbSNP Id: rs1926376576

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078270_18078271del , CM000684.2:g.18078270_18078271del	GRCh38
NC_000022.10:g.18561036_18561037del , CM000684.1:g.18561036_18561037del	GRCh37
NC_000022.9:g.16941036_16941037del	NCBI36
NG_008339.1:g.5351_5352del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-107_-106del MANE Select	ENSP00000382648.4:n.-107_-106del
ENST00000474897.6:c.-81-26_-81-25del	ENSP00000434235.2:n.-81-26_-81-25del
ENST00000329627.11:c.-81-26_-81-25del	ENSP00000331106.5:n.-81-26_-81-25del
ENST00000399744.7:c.-107_-106del	ENSP00000382648.3:n.-107_-106del
ENST00000474897.5:c.-107_-106del	ENSP00000434235.1:n.-107_-106del
ENST00000610387.4:c.-81-26_-81-25del	ENSP00000482091.1:n.-81-26_-81-25del
NM_001127649.2:c.-107_-106del	NP_001121121.1:n.-107_-106del
NM_001199319.1:c.-81-26_-81-25del	NP_001186248.1:n.-81-26_-81-25del
NM_017929.5:c.-81-26_-81-25del	NP_060399.1:n.-81-26_-81-25del
NM_001127649.3:c.-107_-106del MANE Select	NP_001121121.1:n.-107_-106del
NM_001199319.2:c.-81-26_-81-25del	NP_001186248.1:n.-81-26_-81-25del
NM_017929.6:c.-81-26_-81-25del	NP_060399.1:n.-81-26_-81-25del