Canonical Allele Identifier: CA365887500
Gene: PEX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485208T>G , CM000668.2:g.143485208T>G GRCh38
NC_000006.11:g.143806345T>G , CM000668.1:g.143806345T>G GRCh37
NC_000006.10:g.143848038T>G NCBI36
NG_008459.1:g.39428T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.998T>G MANE Select ENSP00000356563.4:p.Ile333Ser
ENST00000367591.4:c.998T>G ENSP00000356563.4:p.Ile333Ser
ENST00000585848.1:n.137T>G
NM_003630.2:c.998T>G NP_003621.1:p.Ile333Ser
NM_003630.3:c.998T>G MANE Select NP_003621.1:p.Ile333Ser