Canonical Allele Identifier: CA399137282
Gene: PEX12 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35576032G>T , CM000679.2:g.35576032G>T GRCh38
NC_000017.10:g.33903051G>T , CM000679.1:g.33903051G>T GRCh37
NC_000017.9:g.30927164G>T NCBI36
NG_008447.1:g.7606C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000225873.9:c.830C>A MANE Select ENSP00000225873.3:p.Thr277Asn
ENST00000586663.2:c.830C>A ENSP00000466894.2:p.Thr277Asn
ENST00000225873.8:c.830C>A ENSP00000225873.3:p.Thr277Asn
ENST00000586663.1:c.830C>A ENSP00000466894.1:p.Thr277Asn
ENST00000613219.4:c.830C>A ENSP00000482609.1:p.Thr277Asn
NM_000286.2:c.830C>A NP_000277.1:p.Thr277Asn
NM_000286.3:c.830C>A MANE Select NP_000277.1:p.Thr277Asn