Canonical Allele Identifier: CA1963455908

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34916453G= , CM000673.2:g.34916453G= GRCh38
NC_000011.9:g.34938000G= , CM000673.1:g.34938000G= GRCh37
NC_000011.8:g.34894576G= NCBI36
NG_013368.1:g.5324G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.-54G= (PDHX) ENSP00000389404.3:n.-54G=
ENST00000395787.3:c.-169C= (APIP) ENSP00000379133.3:n.-169C=
ENST00000448838.7:c.82G= (PDHX) ENSP00000389404.2:p.Glu28=
ENST00000533550.5:c.-21+515G= (PDHX) ENSP00000431281.1:n.-21+515G=
NM_001135024.1:c.82G= (PDHX) NP_001128496.1:p.Glu28=
NM_001166158.1:c.-203G= (PDHX) NP_001159630.1:n.-203G=
NM_003477.2:c.-203G= (PDHX) NP_003468.2:n.-203G=
XM_011520390.1:c.-21+515G= (PDHX) XP_011518692.1:n.-21+515G=
NM_001135024.2:c.-54G= (PDHX) NP_001128496.2:n.-54G=