Canonical Allele Identifier: CA2693251483
Gene: PDHA1 HGNC NCBI

Linked Data

gnomAD v4: X-19359867-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359867A>G , CM000685.2:g.19359867A>G GRCh38
NC_000023.10:g.19377985A>G , CM000685.1:g.19377985A>G GRCh37
NC_000023.9:g.19287906A>G NCBI36
NG_016781.1:g.20975A>G
NG_021184.1:g.160395T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*214A>G ENSP00000348062.6:n.*214A>G
ENST00000423505.6:c.*214A>G ENSP00000406473.2:n.*214A>G
ENST00000696704.1:c.*719A>G ENSP00000512823.1:n.*719A>G
ENST00000696705.1:c.*842A>G ENSP00000512824.1:n.*842A>G
ENST00000422285.7:c.*214A>G MANE Select ENSP00000394382.2:n.*214A>G
ENST00000379806.9:c.*214A>G ENSP00000369134.5:n.*214A>G
ENST00000422285.6:c.*214A>G ENSP00000394382.2:n.*214A>G
ENST00000540249.5:c.*214A>G ENSP00000440761.1:n.*214A>G
ENST00000545074.5:c.*214A>G ENSP00000438550.1:n.*214A>G
NM_000284.3:c.*214A>G NP_000275.1:n.*214A>G
NM_001173454.1:c.*214A>G NP_001166925.1:n.*214A>G
NM_001173455.1:c.*214A>G NP_001166926.1:n.*214A>G
NM_001173456.1:c.*214A>G NP_001166927.1:n.*214A>G
XM_011545531.1:c.*214A>G XP_011543833.1:n.*214A>G
XM_011545532.1:c.*214A>G XP_011543834.1:n.*214A>G
NM_000284.4:c.*214A>G MANE Select NP_000275.1:n.*214A>G
NM_001173454.2:c.*214A>G NP_001166925.1:n.*214A>G
NM_001173455.2:c.*214A>G NP_001166926.1:n.*214A>G
NM_001173456.2:c.*214A>G NP_001166927.1:n.*214A>G