Canonical Allele Identifier: CA2655187175

Gene: PEX26

Linked Data

• gnomAD v4: 22-18080121-TCGGA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.18080122_18080125del , CM000684.2:g.18080122_18080125del	GRCh38
NC_000022.10:g.18562888_18562891del , CM000684.1:g.18562888_18562891del	GRCh37
NC_000022.9:g.16942888_16942891del	NCBI36
NG_008339.1:g.7203_7206del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000399744.8:c.371+108_371+111del MANE Select	ENSP00000382648.4:n.371+108_371+111del
ENST00000474897.6:c.371+108_371+111del	ENSP00000434235.2:n.371+108_371+111del
ENST00000329627.11:c.371+108_371+111del	ENSP00000331106.5:n.371+108_371+111del
ENST00000399744.7:c.371+108_371+111del	ENSP00000382648.3:n.371+108_371+111del
ENST00000428061.2:c.371+108_371+111del	ENSP00000412441.2:n.371+108_371+111del
ENST00000474897.5:c.371+108_371+111del	ENSP00000434235.1:n.371+108_371+111del
ENST00000610387.4:c.371+108_371+111del	ENSP00000482091.1:n.371+108_371+111del
NM_001127649.2:c.371+108_371+111del	NP_001121121.1:n.371+108_371+111del
NM_001199319.1:c.371+108_371+111del	NP_001186248.1:n.371+108_371+111del
NM_017929.5:c.371+108_371+111del	NP_060399.1:n.371+108_371+111del
NM_001127649.3:c.371+108_371+111del MANE Select	NP_001121121.1:n.371+108_371+111del
NM_001199319.2:c.371+108_371+111del	NP_001186248.1:n.371+108_371+111del
NM_017929.6:c.371+108_371+111del	NP_060399.1:n.371+108_371+111del