Canonical Allele Identifier: CA1963422262
Gene: PDHX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34916523G= , CM000673.2:g.34916523G= GRCh38
NC_000011.9:g.34938070G= , CM000673.1:g.34938070G= GRCh37
NC_000011.8:g.34894646G= NCBI36
NG_013368.1:g.5394G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.-21+37G= ENSP00000389404.3:n.-21+37G=
ENST00000448838.7:c.115+37G= ENSP00000389404.2:n.115+37G=
ENST00000533550.5:c.-21+585G= ENSP00000431281.1:n.-21+585G=
NM_001135024.1:c.115+37G= NP_001128496.1:n.115+37G=
NM_001166158.1:c.-133G= NP_001159630.1:n.-133G=
NM_003477.2:c.-133G= NP_003468.2:n.-133G=
XM_011520390.1:c.-21+585G= XP_011518692.1:n.-21+585G=
NM_001135024.2:c.-21+37G= NP_001128496.2:n.-21+37G=