Canonical Allele Identifier: CA2395402884

Gene: PEX26

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078654_18078655delinsTG , CM000684.2:g.18078654_18078655delinsTG	GRCh38
NC_000022.10:g.18561420_18561421delinsTG , CM000684.1:g.18561420_18561421delinsTG	GRCh37
NC_000022.9:g.16941420_16941421delinsTG	NCBI36
NG_008339.1:g.5735_5736delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.230+48_230+49delinsTG MANE Select	ENSP00000382648.4:n.230+48_230+49delinsTG
ENST00000474897.6:c.230+48_230+49delinsTG	ENSP00000434235.2:n.230+48_230+49delinsTG
ENST00000329627.11:c.230+48_230+49delinsTG	ENSP00000331106.5:n.230+48_230+49delinsTG
ENST00000399744.7:c.230+48_230+49delinsTG	ENSP00000382648.3:n.230+48_230+49delinsTG
ENST00000428061.2:c.230+48_230+49delinsTG	ENSP00000412441.2:n.230+48_230+49delinsTG
ENST00000474897.5:c.230+48_230+49delinsTG	ENSP00000434235.1:n.230+48_230+49delinsTG
ENST00000610387.4:c.230+48_230+49delinsTG	ENSP00000482091.1:n.230+48_230+49delinsTG
NM_001127649.2:c.230+48_230+49delinsTG	NP_001121121.1:n.230+48_230+49delinsTG
NM_001199319.1:c.230+48_230+49delinsTG	NP_001186248.1:n.230+48_230+49delinsTG
NM_017929.5:c.230+48_230+49delinsTG	NP_060399.1:n.230+48_230+49delinsTG
NM_001127649.3:c.230+48_230+49delinsTG MANE Select	NP_001121121.1:n.230+48_230+49delinsTG
NM_001199319.2:c.230+48_230+49delinsTG	NP_001186248.1:n.230+48_230+49delinsTG
NM_017929.6:c.230+48_230+49delinsTG	NP_060399.1:n.230+48_230+49delinsTG