Canonical Allele Identifier: CA2506725346
Gene: PDHX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34995897A>T , CM000673.2:g.34995897A>T GRCh38
NC_000011.9:g.35017444A>T , CM000673.1:g.35017444A>T GRCh37
NC_000011.8:g.34974020A>T NCBI36
NG_013368.1:g.84768A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.*725A>T ENSP00000389404.3:n.*725A>T
ENST00000227868.9:c.*725A>T MANE Select ENSP00000227868.4:n.*725A>T
ENST00000227868.8:c.*725A>T ENSP00000227868.4:n.*725A>T
ENST00000448838.7:c.*725A>T ENSP00000389404.2:n.*725A>T
ENST00000477173.3:n.161+3518A>T
NM_001135024.1:c.*725A>T NP_001128496.1:n.*725A>T
NM_001166158.1:c.*725A>T NP_001159630.1:n.*725A>T
NM_003477.2:c.*725A>T NP_003468.2:n.*725A>T
XM_011520390.1:c.*725A>T XP_011518692.1:n.*725A>T
NM_003477.3:c.*725A>T MANE Select NP_003468.2:n.*725A>T
NM_001135024.2:c.*725A>T NP_001128496.2:n.*725A>T
NM_001166158.2:c.*725A>T NP_001159630.1:n.*725A>T