Canonical Allele Identifier: CA452462602
Gene: PEX3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.143806352A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.143485215A>G , CM000668.2:g.143485215A>G GRCh38
NC_000006.11:g.143806352A>G , CM000668.1:g.143806352A>G GRCh37
NC_000006.10:g.143848045A>G NCBI36
NG_008459.1:g.39435A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000367591.5:c.1005A>G MANE Select ENSP00000356563.4:p.Ser335=
ENST00000367591.4:c.1005A>G ENSP00000356563.4:p.Ser335=
ENST00000585848.1:n.144A>G
NM_003630.2:c.1005A>G NP_003621.1:p.Ser335=
NM_003630.3:c.1005A>G MANE Select NP_003621.1:p.Ser335=