Canonical Allele Identifier: CA399137021
Gene: PEX12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35575904A>G , CM000679.2:g.35575904A>G GRCh38
NC_000017.10:g.33902923A>G , CM000679.1:g.33902923A>G GRCh37
NC_000017.9:g.30927036A>G NCBI36
NG_008447.1:g.7734T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.958T>C MANE Select ENSP00000225873.3:p.Ser320Pro
ENST00000586663.2:c.958T>C ENSP00000466894.2:p.Ser320Pro
ENST00000225873.8:c.958T>C ENSP00000225873.3:p.Ser320Pro
ENST00000586663.1:c.958T>C ENSP00000466894.1:p.Ser320Pro
ENST00000613219.4:c.958T>C ENSP00000482609.1:p.Ser320Pro
NM_000286.2:c.958T>C NP_000277.1:p.Ser320Pro
NM_000286.3:c.958T>C MANE Select NP_000277.1:p.Ser320Pro