Canonical Allele Identifier: CA4788652

Gene: PEX2

Linked Data

• ClinVar Variation Id: 1115953
• ClinVar RCV Id: RCV001444167
• dbSNP Id: rs143661965
• ExAC: 8:77895617 G / A
• gnomAD v2: 8-77895617-G-A
• gnomAD v3: 8-76983381-G-A
• gnomAD v4: 8-76983381-G-A
• MyVariant Identifiers: chr8:g.77895617G>A (hg19) ; chr8:g.76983381G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983381G>A , CM000670.2:g.76983381G>A	GRCh38
NC_000008.10:g.77895617G>A , CM000670.1:g.77895617G>A	GRCh37
NC_000008.9:g.78058172G>A	NCBI36
NG_008371.1:g.21908C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357039.9:c.798C>T MANE Select	ENSP00000349543.4:p.Phe266=
ENST00000357039.8:c.798C>T	ENSP00000349543.4:p.Phe266=
ENST00000520103.5:c.798C>T	ENSP00000428590.1:p.Phe266=
ENST00000522527.5:c.798C>T	ENSP00000428638.1:p.Phe266=
NM_000318.2:c.798C>T	NP_000309.1:p.Phe266=
NM_001079867.1:c.798C>T	NP_001073336.1:p.Phe266=
NM_001172086.1:c.798C>T	NP_001165557.1:p.Phe266=
NM_001172087.1:c.798C>T	NP_001165558.1:p.Phe266=
NM_000318.3:c.798C>T MANE Select	NP_000309.2:p.Phe266=
NM_001079867.2:c.798C>T	NP_001073336.2:p.Phe266=
NM_001172086.2:c.798C>T	NP_001165557.2:p.Phe266=
NM_001172087.2:c.798C>T	NP_001165558.2:p.Phe266=