Canonical Allele Identifier: CA2687718792

Gene: PEX2

Linked Data

• gnomAD v4: 8-76983130-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983130C>T , CM000670.2:g.76983130C>T	GRCh38
NC_000008.10:g.77895366C>T , CM000670.1:g.77895366C>T	GRCh37
NC_000008.9:g.78057921C>T	NCBI36
NG_008371.1:g.22159G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357039.9:c.*131G>A MANE Select	ENSP00000349543.4:n.*131G>A
ENST00000357039.8:c.*131G>A	ENSP00000349543.4:n.*131G>A
ENST00000520103.5:c.*131G>A	ENSP00000428590.1:n.*131G>A
ENST00000522527.5:c.*131G>A	ENSP00000428638.1:n.*131G>A
NM_000318.2:c.*131G>A	NP_000309.1:n.*131G>A
NM_001079867.1:c.*131G>A	NP_001073336.1:n.*131G>A
NM_001172086.1:c.*131G>A	NP_001165557.1:n.*131G>A
NM_001172087.1:c.*131G>A	NP_001165558.1:n.*131G>A
NM_000318.3:c.*131G>A MANE Select	NP_000309.2:n.*131G>A
NM_001079867.2:c.*131G>A	NP_001073336.2:n.*131G>A
NM_001172086.2:c.*131G>A	NP_001165557.2:n.*131G>A
NM_001172087.2:c.*131G>A	NP_001165558.2:n.*131G>A