Canonical Allele Identifier: CA1669276785
Gene: PEX3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143489759T= , CM000668.2:g.143489759T= GRCh38
NC_000006.11:g.143810896T= , CM000668.1:g.143810896T= GRCh37
NC_000006.10:g.143852589T= NCBI36
NG_008459.1:g.43979T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367591.5:c.*533T= MANE Select ENSP00000356563.4:n.*533T=
ENST00000367591.4:c.*533T= ENSP00000356563.4:n.*533T=
NM_003630.2:c.*533T= NP_003621.1:n.*533T=
NM_003630.3:c.*533T= MANE Select NP_003621.1:n.*533T=