Canonical Allele Identifier: CA2655182821

Gene: PEX26

Linked Data

• gnomAD v4: 22-18078166-TA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18078169del , CM000684.2:g.18078169del	GRCh38
NC_000022.10:g.18560935del , CM000684.1:g.18560935del	GRCh37
NC_000022.9:g.16940935del	NCBI36
NG_008339.1:g.5250del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.-208del MANE Select	ENSP00000382648.4:n.-208del
ENST00000474897.6:c.-82+122del	ENSP00000434235.2:n.-82+122del
ENST00000329627.11:c.-82+122del	ENSP00000331106.5:n.-82+122del
ENST00000399744.7:c.-208del	ENSP00000382648.3:n.-208del
ENST00000474897.5:c.-208del	ENSP00000434235.1:n.-208del
ENST00000610387.4:c.-82+122del	ENSP00000482091.1:n.-82+122del
NM_001127649.2:c.-208del	NP_001121121.1:n.-208del
NM_001199319.1:c.-82+122del	NP_001186248.1:n.-82+122del
NM_017929.5:c.-82+122del	NP_060399.1:n.-82+122del
NM_001127649.3:c.-208del MANE Select	NP_001121121.1:n.-208del
NM_001199319.2:c.-82+122del	NP_001186248.1:n.-82+122del
NM_017929.6:c.-82+122del	NP_060399.1:n.-82+122del