Canonical Allele Identifier: CA499903588
Gene: PEX12 HGNC NCBI

Linked Data

MyVariant Identifiers: chr17:g.33904470T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35577451T>C , CM000679.2:g.35577451T>C GRCh38
NC_000017.10:g.33904470T>C , CM000679.1:g.33904470T>C GRCh37
NC_000017.9:g.30928583T>C NCBI36
NG_008447.1:g.6187A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.267A>G MANE Select ENSP00000225873.3:p.Leu89=
ENST00000586663.2:c.267A>G ENSP00000466894.2:p.Leu89=
ENST00000225873.8:c.267A>G ENSP00000225873.3:p.Leu89=
ENST00000585380.1:c.267A>G ENSP00000466280.1:p.Leu89=
ENST00000586663.1:c.267A>G ENSP00000466894.1:p.Leu89=
ENST00000613219.4:c.267A>G ENSP00000482609.1:p.Leu89=
NM_000286.2:c.267A>G NP_000277.1:p.Leu89=
NM_000286.3:c.267A>G MANE Select NP_000277.1:p.Leu89=
Search 100 bp 5'
Search 100 bp 3'