Canonical Allele Identifier: CA2257586236
Gene: PEX12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575811G= , CM000679.2:g.35575811G= GRCh38
NC_000017.10:g.33902830G= , CM000679.1:g.33902830G= GRCh37
NC_000017.9:g.30926943G= NCBI36
NG_008447.1:g.7827C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.1051C= MANE Select ENSP00000225873.3:p.Leu351=
ENST00000586663.2:c.1051C= ENSP00000466894.2:p.Leu351=
ENST00000225873.8:c.1051C= ENSP00000225873.3:p.Leu351=
ENST00000586663.1:c.1051C= ENSP00000466894.1:p.Leu351=
ENST00000613219.4:c.1051C= ENSP00000482609.1:p.Leu351=
NM_000286.2:c.1051C= NP_000277.1:p.Leu351=
NM_000286.3:c.1051C= MANE Select NP_000277.1:p.Leu351=