Canonical Allele Identifier: CA2257586430
Gene: PEX12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575920A= , CM000679.2:g.35575920A= GRCh38
NC_000017.10:g.33902939A= , CM000679.1:g.33902939A= GRCh37
NC_000017.9:g.30927052A= NCBI36
NG_008447.1:g.7718T=

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.942T= MANE Select ENSP00000225873.3:p.Asp314=
ENST00000586663.2:c.942T= ENSP00000466894.2:p.Asp314=
ENST00000225873.8:c.942T= ENSP00000225873.3:p.Asp314=
ENST00000586663.1:c.942T= ENSP00000466894.1:p.Asp314=
ENST00000613219.4:c.942T= ENSP00000482609.1:p.Asp314=
NM_000286.2:c.942T= NP_000277.1:p.Asp314=
NM_000286.3:c.942T= MANE Select NP_000277.1:p.Asp314=