Canonical Allele Identifier: CA1669274511
Gene: PEX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485192A= , CM000668.2:g.143485192A= GRCh38
NC_000006.11:g.143806329A= , CM000668.1:g.143806329A= GRCh37
NC_000006.10:g.143848022A= NCBI36
NG_008459.1:g.39412A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.982A= MANE Select ENSP00000356563.4:p.Ile328=
ENST00000367591.4:c.982A= ENSP00000356563.4:p.Ile328=
ENST00000585848.1:n.121A=
NM_003630.2:c.982A= NP_003621.1:p.Ile328=
NM_003630.3:c.982A= MANE Select NP_003621.1:p.Ile328=