Canonical Allele Identifier: CA2687718864

Gene: PEX2

Linked Data

• gnomAD v4: 8-76983588-CCA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983589_76983590del , CM000670.2:g.76983589_76983590del	GRCh38
NC_000008.10:g.77895825_77895826del , CM000670.1:g.77895825_77895826del	GRCh37
NC_000008.9:g.78058380_78058381del	NCBI36
NG_008371.1:g.21699_21700del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357039.9:c.589_590del MANE Select	ENSP00000349543.4:p.Trp197AlafsTer5
ENST00000357039.8:c.589_590del	ENSP00000349543.4:p.Trp197AlafsTer5
ENST00000520103.5:c.589_590del	ENSP00000428590.1:p.Trp197AlafsTer5
ENST00000522527.5:c.589_590del	ENSP00000428638.1:p.Trp197AlafsTer5
NM_000318.2:c.589_590del	NP_000309.1:p.Trp197AlafsTer5
NM_001079867.1:c.589_590del	NP_001073336.1:p.Trp197AlafsTer5
NM_001172086.1:c.589_590del	NP_001165557.1:p.Trp197AlafsTer5
NM_001172087.1:c.589_590del	NP_001165558.1:p.Trp197AlafsTer5
NM_000318.3:c.589_590del MANE Select	NP_000309.2:p.Trp197AlafsTer5
NM_001079867.2:c.589_590del	NP_001073336.2:p.Trp197AlafsTer5
NM_001172086.2:c.589_590del	NP_001165557.2:p.Trp197AlafsTer5
NM_001172087.2:c.589_590del	NP_001165558.2:p.Trp197AlafsTer5