Canonical Allele Identifier: CA2257587002
Gene: PEX12 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35576275A= , CM000679.2:g.35576275A= GRCh38
NC_000017.10:g.33903294A= , CM000679.1:g.33903294A= GRCh37
NC_000017.9:g.30927407A= NCBI36
NG_008447.1:g.7363T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225873.9:c.681-94T= MANE Select ENSP00000225873.3:n.681-94T=
ENST00000586663.2:c.681-94T= ENSP00000466894.2:n.681-94T=
ENST00000225873.8:c.681-94T= ENSP00000225873.3:n.681-94T=
ENST00000586663.1:c.681-94T= ENSP00000466894.1:n.681-94T=
ENST00000613219.4:c.681-94T= ENSP00000482609.1:n.681-94T=
NM_000286.2:c.681-94T= NP_000277.1:n.681-94T=
NM_000286.3:c.681-94T= MANE Select NP_000277.1:n.681-94T=
Search 100 bp 5'
Search 100 bp 3'