Canonical Allele Identifier: CA365887465
Gene: PEX3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485202G>C , CM000668.2:g.143485202G>C GRCh38
NC_000006.11:g.143806339G>C , CM000668.1:g.143806339G>C GRCh37
NC_000006.10:g.143848032G>C NCBI36
NG_008459.1:g.39422G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.992G>C MANE Select ENSP00000356563.4:p.Gly331Ala
ENST00000367591.4:c.992G>C ENSP00000356563.4:p.Gly331Ala
ENST00000585848.1:n.131G>C
NM_003630.2:c.992G>C NP_003621.1:p.Gly331Ala
NM_003630.3:c.992G>C MANE Select NP_003621.1:p.Gly331Ala