Canonical Allele Identifier: CA365887459
Gene: PEX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485201G>T , CM000668.2:g.143485201G>T GRCh38
NC_000006.11:g.143806338G>T , CM000668.1:g.143806338G>T GRCh37
NC_000006.10:g.143848031G>T NCBI36
NG_008459.1:g.39421G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.991G>T MANE Select ENSP00000356563.4:p.Gly331Ter
ENST00000367591.4:c.991G>T ENSP00000356563.4:p.Gly331Ter
ENST00000585848.1:n.130G>T
NM_003630.2:c.991G>T NP_003621.1:p.Gly331Ter
NM_003630.3:c.991G>T MANE Select NP_003621.1:p.Gly331Ter