Canonical Allele Identifier: CA1095333755
Gene: PEX3 HGNC NCBI

Linked Data

dbSNP Id: rs1780297770

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485112del , CM000668.2:g.143485112del GRCh38
NC_000006.11:g.143806249del , CM000668.1:g.143806249del GRCh37
NC_000006.10:g.143847942del NCBI36
NG_008459.1:g.39332del

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.942-40del MANE Select ENSP00000356563.4:n.942-40del
ENST00000367591.4:c.942-40del ENSP00000356563.4:n.942-40del
ENST00000585848.1:n.41del
NM_003630.2:c.942-40del NP_003621.1:n.942-40del
NM_003630.3:c.942-40del MANE Select NP_003621.1:n.942-40del