Canonical Allele Identifier: CA399136794
Gene: PEX12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575803T>G , CM000679.2:g.35575803T>G GRCh38
NC_000017.10:g.33902822T>G , CM000679.1:g.33902822T>G GRCh37
NC_000017.9:g.30926935T>G NCBI36
NG_008447.1:g.7835A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.1059A>C MANE Select ENSP00000225873.3:p.Lys353Asn
ENST00000586663.2:c.1059A>C ENSP00000466894.2:p.Lys353Asn
ENST00000225873.8:c.1059A>C ENSP00000225873.3:p.Lys353Asn
ENST00000586663.1:c.1059A>C ENSP00000466894.1:p.Lys353Asn
ENST00000613219.4:c.1059A>C ENSP00000482609.1:p.Lys353Asn
NM_000286.2:c.1059A>C NP_000277.1:p.Lys353Asn
NM_000286.3:c.1059A>C MANE Select NP_000277.1:p.Lys353Asn