Canonical Allele Identifier: CA399137043
Gene: PEX12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575916C>A , CM000679.2:g.35575916C>A GRCh38
NC_000017.10:g.33902935C>A , CM000679.1:g.33902935C>A GRCh37
NC_000017.9:g.30927048C>A NCBI36
NG_008447.1:g.7722G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.946G>T MANE Select ENSP00000225873.3:p.Val316Phe
ENST00000586663.2:c.946G>T ENSP00000466894.2:p.Val316Phe
ENST00000225873.8:c.946G>T ENSP00000225873.3:p.Val316Phe
ENST00000586663.1:c.946G>T ENSP00000466894.1:p.Val316Phe
ENST00000613219.4:c.946G>T ENSP00000482609.1:p.Val316Phe
NM_000286.2:c.946G>T NP_000277.1:p.Val316Phe
NM_000286.3:c.946G>T MANE Select NP_000277.1:p.Val316Phe