Canonical Allele Identifier: CA2257586655

Gene: PEX12

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35576051C= , CM000679.2:g.35576051C=	GRCh38
NC_000017.10:g.33903070C= , CM000679.1:g.33903070C=	GRCh37
NC_000017.9:g.30927183C=	NCBI36
NG_008447.1:g.7587G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000225873.9:c.811G= MANE Select	ENSP00000225873.3:p.Glu271=
ENST00000586663.2:c.811G=	ENSP00000466894.2:p.Glu271=
ENST00000225873.8:c.811G=	ENSP00000225873.3:p.Glu271=
ENST00000586663.1:c.811G=	ENSP00000466894.1:p.Glu271=
ENST00000613219.4:c.811G=	ENSP00000482609.1:p.Glu271=
NM_000286.2:c.811G=	NP_000277.1:p.Glu271=
NM_000286.3:c.811G= MANE Select	NP_000277.1:p.Glu271=