Canonical Allele Identifier: CA399136798
Gene: PEX12 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.1057A>T MANE Select ENSP00000225873.3:p.Lys353Ter
ENST00000586663.2:c.1057A>T ENSP00000466894.2:p.Lys353Ter
ENST00000225873.8:c.1057A>T ENSP00000225873.3:p.Lys353Ter
ENST00000586663.1:c.1057A>T ENSP00000466894.1:p.Lys353Ter
ENST00000613219.4:c.1057A>T ENSP00000482609.1:p.Lys353Ter
NM_000286.2:c.1057A>T NP_000277.1:p.Lys353Ter
NM_000286.3:c.1057A>T MANE Select NP_000277.1:p.Lys353Ter