Canonical Allele Identifier: CA2818335308

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18080186del , CM000684.2:g.18080186del	GRCh38
NC_000022.10:g.18562952del , CM000684.1:g.18562952del	GRCh37
NC_000022.9:g.16942952del	NCBI36
NG_008339.1:g.7267del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.371+172del MANE Select	ENSP00000382648.4:n.371+172del
ENST00000474897.6:c.371+172del	ENSP00000434235.2:n.371+172del
ENST00000329627.11:c.371+172del	ENSP00000331106.5:n.371+172del
ENST00000399744.7:c.371+172del	ENSP00000382648.3:n.371+172del
ENST00000428061.2:c.371+172del	ENSP00000412441.2:n.371+172del
ENST00000474897.5:c.371+172del	ENSP00000434235.1:n.371+172del
ENST00000610387.4:c.371+172del	ENSP00000482091.1:n.371+172del
NM_001127649.2:c.371+172del	NP_001121121.1:n.371+172del
NM_001199319.1:c.371+172del	NP_001186248.1:n.371+172del
NM_017929.5:c.371+172del	NP_060399.1:n.371+172del
NM_001127649.3:c.371+172del MANE Select	NP_001121121.1:n.371+172del
NM_001199319.2:c.371+172del	NP_001186248.1:n.371+172del
NM_017929.6:c.371+172del	NP_060399.1:n.371+172del