Canonical Allele Identifier: CA399137038
Gene: PEX12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575913G>T , CM000679.2:g.35575913G>T GRCh38
NC_000017.10:g.33902932G>T , CM000679.1:g.33902932G>T GRCh37
NC_000017.9:g.30927045G>T NCBI36
NG_008447.1:g.7725C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.949C>A MANE Select ENSP00000225873.3:p.Leu317Ile
ENST00000586663.2:c.949C>A ENSP00000466894.2:p.Leu317Ile
ENST00000225873.8:c.949C>A ENSP00000225873.3:p.Leu317Ile
ENST00000586663.1:c.949C>A ENSP00000466894.1:p.Leu317Ile
ENST00000613219.4:c.949C>A ENSP00000482609.1:p.Leu317Ile
NM_000286.2:c.949C>A NP_000277.1:p.Leu317Ile
NM_000286.3:c.949C>A MANE Select NP_000277.1:p.Leu317Ile