Canonical Allele Identifier: CA2257586658
Gene: PEX12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35576052T= , CM000679.2:g.35576052T= GRCh38
NC_000017.10:g.33903071T= , CM000679.1:g.33903071T= GRCh37
NC_000017.9:g.30927184T= NCBI36
NG_008447.1:g.7586A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225873.9:c.810A= MANE Select ENSP00000225873.3:p.Gln270=
ENST00000586663.2:c.810A= ENSP00000466894.2:p.Gln270=
ENST00000225873.8:c.810A= ENSP00000225873.3:p.Gln270=
ENST00000586663.1:c.810A= ENSP00000466894.1:p.Gln270=
ENST00000613219.4:c.810A= ENSP00000482609.1:p.Gln270=
NM_000286.2:c.810A= NP_000277.1:p.Gln270=
NM_000286.3:c.810A= MANE Select NP_000277.1:p.Gln270=