Canonical Allele Identifier: CA2257586137
Gene: PEX12 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575733G= , CM000679.2:g.35575733G= GRCh38
NC_000017.10:g.33902752G= , CM000679.1:g.33902752G= GRCh37
NC_000017.9:g.30926865G= NCBI36
NG_008447.1:g.7905C=

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.*49C= MANE Select ENSP00000225873.3:n.*49C=
ENST00000225873.8:c.*49C= ENSP00000225873.3:n.*49C=
ENST00000613219.4:c.*49C= ENSP00000482609.1:n.*49C=
NM_000286.2:c.*49C= NP_000277.1:n.*49C=
NM_000286.3:c.*49C= MANE Select NP_000277.1:n.*49C=