Canonical Allele Identifier: CA1963422410
Gene: PDHX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34916610T= , CM000673.2:g.34916610T= GRCh38
NC_000011.9:g.34938157T= , CM000673.1:g.34938157T= GRCh37
NC_000011.8:g.34894733T= NCBI36
NG_013368.1:g.5481T=

Transcript Alleles

HGVS Amino-acid change
ENST00000448838.8:c.-21+124T= ENSP00000389404.3:n.-21+124T=
ENST00000227868.8:c.-46T= ENSP00000227868.4:n.-46T=
ENST00000448838.7:c.115+124T= ENSP00000389404.2:n.115+124T=
ENST00000533550.5:c.-21+672T= ENSP00000431281.1:n.-21+672T=
NM_001135024.1:c.115+124T= NP_001128496.1:n.115+124T=
NM_001166158.1:c.-46T= NP_001159630.1:n.-46T=
NM_003477.2:c.-46T= NP_003468.2:n.-46T=
XM_011520390.1:c.-21+672T= XP_011518692.1:n.-21+672T=
NM_001135024.2:c.-21+124T= NP_001128496.2:n.-21+124T=