Canonical Allele Identifier: CA371556628

Gene: PEX2

Linked Data

• ClinVar Variation Id: 1381225
• ClinVar RCV Id: RCV001921899
• dbSNP Id: rs1220452895
• MyVariant Identifiers: chr8:g.77895649T>C (hg19) ; chr8:g.76983413T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.76983413T>C , CM000670.2:g.76983413T>C	GRCh38
NC_000008.10:g.77895649T>C , CM000670.1:g.77895649T>C	GRCh37
NC_000008.9:g.78058204T>C	NCBI36
NG_008371.1:g.21876A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000357039.9:c.766A>G MANE Select	ENSP00000349543.4:p.Thr256Ala
ENST00000357039.8:c.766A>G	ENSP00000349543.4:p.Thr256Ala
ENST00000520103.5:c.766A>G	ENSP00000428590.1:p.Thr256Ala
ENST00000522527.5:c.766A>G	ENSP00000428638.1:p.Thr256Ala
NM_000318.2:c.766A>G	NP_000309.1:p.Thr256Ala
NM_001079867.1:c.766A>G	NP_001073336.1:p.Thr256Ala
NM_001172086.1:c.766A>G	NP_001165557.1:p.Thr256Ala
NM_001172087.1:c.766A>G	NP_001165558.1:p.Thr256Ala
NM_000318.3:c.766A>G MANE Select	NP_000309.2:p.Thr256Ala
NM_001079867.2:c.766A>G	NP_001073336.2:p.Thr256Ala
NM_001172086.2:c.766A>G	NP_001165557.2:p.Thr256Ala
NM_001172087.2:c.766A>G	NP_001165558.2:p.Thr256Ala