Canonical Allele Identifier: CA2395402726

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078403_18078404delinsAG , CM000684.2:g.18078403_18078404delinsAG	GRCh38
NC_000022.10:g.18561169_18561170delinsAG , CM000684.1:g.18561169_18561170delinsAG	GRCh37
NC_000022.9:g.16941169_16941170delinsAG	NCBI36
NG_008339.1:g.5484_5485delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.27_28delinsAG MANE Select	ENSP00000382648.4:p.Ala9=
ENST00000474897.6:c.27_28delinsAG	ENSP00000434235.2:p.Ala9=
ENST00000329627.11:c.27_28delinsAG	ENSP00000331106.5:p.Ala9=
ENST00000399744.7:c.27_28delinsAG	ENSP00000382648.3:p.Ala9=
ENST00000428061.2:c.27_28delinsAG	ENSP00000412441.2:p.Ala9=
ENST00000474897.5:c.27_28delinsAG	ENSP00000434235.1:p.Ala9=
ENST00000610387.4:c.27_28delinsAG	ENSP00000482091.1:p.Ala9=
NM_001127649.2:c.27_28delinsAG	NP_001121121.1:p.Ala9=
NM_001199319.1:c.27_28delinsAG	NP_001186248.1:p.Ala9=
NM_017929.5:c.27_28delinsAG	NP_060399.1:p.Ala9=
NM_001127649.3:c.27_28delinsAG MANE Select	NP_001121121.1:p.Ala9=
NM_001199319.2:c.27_28delinsAG	NP_001186248.1:p.Ala9=
NM_017929.6:c.27_28delinsAG	NP_060399.1:p.Ala9=