Canonical Allele Identifier: CA179988238

Gene: PEX2

Linked Data

• ClinVar Variation Id: 1697995
• ClinVar RCV Id: RCV002269418
• dbSNP Id: rs113776305
• gnomAD v2: 8-77895360-G-C
• gnomAD v3: 8-76983124-G-C
• gnomAD v4: 8-76983124-G-C
• MyVariant Identifiers: chr8:g.77895360G>C (hg19) ; chr8:g.76983124G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983124G>C , CM000670.2:g.76983124G>C	GRCh38
NC_000008.10:g.77895360G>C , CM000670.1:g.77895360G>C	GRCh37
NC_000008.9:g.78057915G>C	NCBI36
NG_008371.1:g.22165C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357039.9:c.*137C>G MANE Select	ENSP00000349543.4:n.*137C>G
ENST00000357039.8:c.*137C>G	ENSP00000349543.4:n.*137C>G
ENST00000520103.5:c.*137C>G	ENSP00000428590.1:n.*137C>G
ENST00000522527.5:c.*137C>G	ENSP00000428638.1:n.*137C>G
NM_000318.2:c.*137C>G	NP_000309.1:n.*137C>G
NM_001079867.1:c.*137C>G	NP_001073336.1:n.*137C>G
NM_001172086.1:c.*137C>G	NP_001165557.1:n.*137C>G
NM_001172087.1:c.*137C>G	NP_001165558.1:n.*137C>G
NM_000318.3:c.*137C>G MANE Select	NP_000309.2:n.*137C>G
NM_001079867.2:c.*137C>G	NP_001073336.2:n.*137C>G
NM_001172086.2:c.*137C>G	NP_001165557.2:n.*137C>G
NM_001172087.2:c.*137C>G	NP_001165558.2:n.*137C>G