Canonical Allele Identifier: CA4029509

Gene: PEX3

Linked Data

• ClinVar Variation Id: 355575
• ClinVar RCV Id: RCV000361936 ; RCV000676116
• dbSNP Id: rs35220041
• ExAC: 6:143784092 A / G
• gnomAD v2: 6-143784092-A-G
• gnomAD v3: 6-143462955-A-G
• gnomAD v4: 6-143462955-A-G
• MyVariant Identifiers: chr6:g.143784092A>G (hg19) ; chr6:g.143462955A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.143462955A>G , CM000668.2:g.143462955A>G	GRCh38
NC_000006.11:g.143784092A>G , CM000668.1:g.143784092A>G	GRCh37
NC_000006.10:g.143825785A>G	NCBI36
NG_008459.1:g.17175A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367591.5:c.245A>G MANE Select	ENSP00000356563.4:p.Gln82Arg
ENST00000367591.4:c.245A>G	ENSP00000356563.4:p.Gln82Arg
ENST00000367592.5:c.113A>G	ENSP00000356564.1:p.Gln38Arg
NM_003630.2:c.245A>G	NP_003621.1:p.Gln82Arg
NM_003630.3:c.245A>G MANE Select	NP_003621.1:p.Gln82Arg