Canonical Allele Identifier: CA1963422133

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.34916470A= , CM000673.2:g.34916470A= GRCh38
NC_000011.9:g.34938017A= , CM000673.1:g.34938017A= GRCh37
NC_000011.8:g.34894593A= NCBI36
NG_013368.1:g.5341A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000448838.8:c.-37A= (PDHX) ENSP00000389404.3:n.-37A=
ENST00000395787.3:c.-186T= (APIP) ENSP00000379133.3:n.-186T=
ENST00000448838.7:c.99A= (PDHX) ENSP00000389404.2:p.Ala33=
ENST00000533550.5:c.-21+532A= (PDHX) ENSP00000431281.1:n.-21+532A=
NM_001135024.1:c.99A= (PDHX) NP_001128496.1:p.Ala33=
NM_001166158.1:c.-186A= (PDHX) NP_001159630.1:n.-186A=
NM_003477.2:c.-186A= (PDHX) NP_003468.2:n.-186A=
XM_011520390.1:c.-21+532A= (PDHX) XP_011518692.1:n.-21+532A=
NM_001135024.2:c.-37A= (PDHX) NP_001128496.2:n.-37A=