Canonical Allele Identifier: CA2257586991
Gene: PEX12 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35576239A= , CM000679.2:g.35576239A= GRCh38
NC_000017.10:g.33903258A= , CM000679.1:g.33903258A= GRCh37
NC_000017.9:g.30927371A= NCBI36
NG_008447.1:g.7399T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225873.9:c.681-58T= MANE Select ENSP00000225873.3:n.681-58T=
ENST00000586663.2:c.681-58T= ENSP00000466894.2:n.681-58T=
ENST00000225873.8:c.681-58T= ENSP00000225873.3:n.681-58T=
ENST00000586663.1:c.681-58T= ENSP00000466894.1:n.681-58T=
ENST00000613219.4:c.681-58T= ENSP00000482609.1:n.681-58T=
NM_000286.2:c.681-58T= NP_000277.1:n.681-58T=
NM_000286.3:c.681-58T= MANE Select NP_000277.1:n.681-58T=
Search 100 bp 5'
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