Canonical Allele Identifier: CA1963422195
Gene: PDHX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34916504G= , CM000673.2:g.34916504G= GRCh38
NC_000011.9:g.34938051G= , CM000673.1:g.34938051G= GRCh37
NC_000011.8:g.34894627G= NCBI36
NG_013368.1:g.5375G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.-21+18G= ENSP00000389404.3:n.-21+18G=
ENST00000448838.7:c.115+18G= ENSP00000389404.2:n.115+18G=
ENST00000533550.5:c.-21+566G= ENSP00000431281.1:n.-21+566G=
NM_001135024.1:c.115+18G= NP_001128496.1:n.115+18G=
NM_001166158.1:c.-152G= NP_001159630.1:n.-152G=
NM_003477.2:c.-152G= NP_003468.2:n.-152G=
XM_011520390.1:c.-21+566G= XP_011518692.1:n.-21+566G=
NM_001135024.2:c.-21+18G= NP_001128496.2:n.-21+18G=