Canonical Allele Identifier: CA371556735

Gene: PEX2

Linked Data

• ClinVar Variation Id: 566773
• ClinVar RCV Id: RCV000686680 ; RCV001829894
• dbSNP Id: rs1264938864
• gnomAD v2: 8-77895699-G-A
• gnomAD v3: 8-76983463-G-A
• gnomAD v4: 8-76983463-G-A
• MyVariant Identifiers: chr8:g.77895699G>A (hg19) ; chr8:g.76983463G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983463G>A , CM000670.2:g.76983463G>A	GRCh38
NC_000008.10:g.77895699G>A , CM000670.1:g.77895699G>A	GRCh37
NC_000008.9:g.78058254G>A	NCBI36
NG_008371.1:g.21826C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000357039.9:c.716C>T MANE Select	ENSP00000349543.4:p.Thr239Ile
ENST00000357039.8:c.716C>T	ENSP00000349543.4:p.Thr239Ile
ENST00000520103.5:c.716C>T	ENSP00000428590.1:p.Thr239Ile
ENST00000522527.5:c.716C>T	ENSP00000428638.1:p.Thr239Ile
NM_000318.2:c.716C>T	NP_000309.1:p.Thr239Ile
NM_001079867.1:c.716C>T	NP_001073336.1:p.Thr239Ile
NM_001172086.1:c.716C>T	NP_001165557.1:p.Thr239Ile
NM_001172087.1:c.716C>T	NP_001165558.1:p.Thr239Ile
NM_000318.3:c.716C>T MANE Select	NP_000309.2:p.Thr239Ile
NM_001079867.2:c.716C>T	NP_001073336.2:p.Thr239Ile
NM_001172086.2:c.716C>T	NP_001165557.2:p.Thr239Ile
NM_001172087.2:c.716C>T	NP_001165558.2:p.Thr239Ile