Canonical Allele Identifier: CA1963455900

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34916449G= , CM000673.2:g.34916449G= GRCh38
NC_000011.9:g.34937996G= , CM000673.1:g.34937996G= GRCh37
NC_000011.8:g.34894572G= NCBI36
NG_013368.1:g.5320G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.-58G= (PDHX) ENSP00000389404.3:n.-58G=
ENST00000395787.3:c.-165C= (APIP) ENSP00000379133.3:n.-165C=
ENST00000448838.7:c.78G= (PDHX) ENSP00000389404.2:p.Pro26=
ENST00000533550.5:c.-21+511G= (PDHX) ENSP00000431281.1:n.-21+511G=
NM_001135024.1:c.78G= (PDHX) NP_001128496.1:p.Pro26=
NM_001166158.1:c.-207G= (PDHX) NP_001159630.1:n.-207G=
NM_003477.2:c.-207G= (PDHX) NP_003468.2:n.-207G=
XM_011520390.1:c.-21+511G= (PDHX) XP_011518692.1:n.-21+511G=
NM_001135024.2:c.-58G= (PDHX) NP_001128496.2:n.-58G=