Canonical Allele Identifier: CA399137091
Gene: PEX12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.33902959G>T (hg19) chr17:g.35575940G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575940G>T , CM000679.2:g.35575940G>T GRCh38
NC_000017.10:g.33902959G>T , CM000679.1:g.33902959G>T GRCh37
NC_000017.9:g.30927072G>T NCBI36
NG_008447.1:g.7698C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.922C>A MANE Select ENSP00000225873.3:p.Arg308Ser
ENST00000586663.2:c.922C>A ENSP00000466894.2:p.Arg308Ser
ENST00000225873.8:c.922C>A ENSP00000225873.3:p.Arg308Ser
ENST00000586663.1:c.922C>A ENSP00000466894.1:p.Arg308Ser
ENST00000613219.4:c.922C>A ENSP00000482609.1:p.Arg308Ser
NM_000286.2:c.922C>A NP_000277.1:p.Arg308Ser
NM_000286.3:c.922C>A MANE Select NP_000277.1:p.Arg308Ser
Search 100 bp 5'
Search 100 bp 3'