Canonical Allele Identifier: CA1963455873

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34916440G= , CM000673.2:g.34916440G= GRCh38
NC_000011.9:g.34937987G= , CM000673.1:g.34937987G= GRCh37
NC_000011.8:g.34894563G= NCBI36
NG_013368.1:g.5311G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.-67G= (PDHX) ENSP00000389404.3:n.-67G=
ENST00000395787.3:c.-156C= (APIP) ENSP00000379133.3:n.-156C=
ENST00000448838.7:c.69G= (PDHX) ENSP00000389404.2:p.Lys23=
ENST00000533550.5:c.-21+502G= (PDHX) ENSP00000431281.1:n.-21+502G=
NM_001135024.1:c.69G= (PDHX) NP_001128496.1:p.Lys23=
NM_001166158.1:c.-216G= (PDHX) NP_001159630.1:n.-216G=
NM_003477.2:c.-216G= (PDHX) NP_003468.2:n.-216G=
XM_011520390.1:c.-21+502G= (PDHX) XP_011518692.1:n.-21+502G=
NM_001135024.2:c.-67G= (PDHX) NP_001128496.2:n.-67G=