Canonical Allele Identifier: CA2418225898
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19360011A= , CM000685.2:g.19360011A= GRCh38
NC_000023.10:g.19378129A= , CM000685.1:g.19378129A= GRCh37
NC_000023.9:g.19288050A= NCBI36
NG_016781.1:g.21119A=
NG_021184.1:g.160251T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*358A= ENSP00000348062.6:n.*358A=
ENST00000423505.6:c.*358A= ENSP00000406473.2:n.*358A=
ENST00000696704.1:c.*863A= ENSP00000512823.1:n.*863A=
ENST00000696705.1:c.*986A= ENSP00000512824.1:n.*986A=
ENST00000422285.7:c.*358A= MANE Select ENSP00000394382.2:n.*358A=
ENST00000379806.9:c.*358A= ENSP00000369134.5:n.*358A=
ENST00000422285.6:c.*358A= ENSP00000394382.2:n.*358A=
ENST00000540249.5:c.*358A= ENSP00000440761.1:n.*358A=
ENST00000545074.5:c.*358A= ENSP00000438550.1:n.*358A=
NM_000284.3:c.*358A= NP_000275.1:n.*358A=
NM_001173454.1:c.*358A= NP_001166925.1:n.*358A=
NM_001173455.1:c.*358A= NP_001166926.1:n.*358A=
NM_001173456.1:c.*358A= NP_001166927.1:n.*358A=
XM_011545531.1:c.*358A= XP_011543833.1:n.*358A=
XM_011545532.1:c.*358A= XP_011543834.1:n.*358A=
NM_000284.4:c.*358A= MANE Select NP_000275.1:n.*358A=
NM_001173454.2:c.*358A= NP_001166925.1:n.*358A=
NM_001173455.2:c.*358A= NP_001166926.1:n.*358A=
NM_001173456.2:c.*358A= NP_001166927.1:n.*358A=