Canonical Allele Identifier: CA399137095
Gene: PEX12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.33902961C>A (hg19) chr17:g.35575942C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575942C>A , CM000679.2:g.35575942C>A GRCh38
NC_000017.10:g.33902961C>A , CM000679.1:g.33902961C>A GRCh37
NC_000017.9:g.30927074C>A NCBI36
NG_008447.1:g.7696G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000225873.9:c.920G>T MANE Select ENSP00000225873.3:p.Cys307Phe
ENST00000586663.2:c.920G>T ENSP00000466894.2:p.Cys307Phe
ENST00000225873.8:c.920G>T ENSP00000225873.3:p.Cys307Phe
ENST00000586663.1:c.920G>T ENSP00000466894.1:p.Cys307Phe
ENST00000613219.4:c.920G>T ENSP00000482609.1:p.Cys307Phe
NM_000286.2:c.920G>T NP_000277.1:p.Cys307Phe
NM_000286.3:c.920G>T MANE Select NP_000277.1:p.Cys307Phe
Search 100 bp 5'
Search 100 bp 3'