Canonical Allele Identifier: CA399136799
Gene: PEX12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575805T>G , CM000679.2:g.35575805T>G GRCh38
NC_000017.10:g.33902824T>G , CM000679.1:g.33902824T>G GRCh37
NC_000017.9:g.30926937T>G NCBI36
NG_008447.1:g.7833A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.1057A>C MANE Select ENSP00000225873.3:p.Lys353Gln
ENST00000586663.2:c.1057A>C ENSP00000466894.2:p.Lys353Gln
ENST00000225873.8:c.1057A>C ENSP00000225873.3:p.Lys353Gln
ENST00000586663.1:c.1057A>C ENSP00000466894.1:p.Lys353Gln
ENST00000613219.4:c.1057A>C ENSP00000482609.1:p.Lys353Gln
NM_000286.2:c.1057A>C NP_000277.1:p.Lys353Gln
NM_000286.3:c.1057A>C MANE Select NP_000277.1:p.Lys353Gln