Canonical Allele Identifier: CA2693250537
Gene: PDHA1 HGNC NCBI

Linked Data

gnomAD v4: X-19355659-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19355659C>T , CM000685.2:g.19355659C>T GRCh38
NC_000023.10:g.19373777C>T , CM000685.1:g.19373777C>T GRCh37
NC_000023.9:g.19283698C>T NCBI36
NG_016781.1:g.16767C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.781-27C>T ENSP00000348062.6:n.781-27C>T
ENST00000379805.4:c.*452-27C>T ENSP00000369133.3:n.*452-27C>T
ENST00000417819.6:c.844-27C>T ENSP00000404616.2:n.844-27C>T
ENST00000423505.6:c.874-27C>T ENSP00000406473.2:n.874-27C>T
ENST00000481733.2:n.555-27C>T
ENST00000696704.1:c.*92-27C>T ENSP00000512823.1:n.*92-27C>T
ENST00000696705.1:c.*215-27C>T ENSP00000512824.1:n.*215-27C>T
ENST00000422285.7:c.760-27C>T MANE Select ENSP00000394382.2:n.760-27C>T
ENST00000379804.1:c.-111C>T ENSP00000369132.1:n.-111C>T
ENST00000379806.9:c.874-27C>T ENSP00000369134.5:n.874-27C>T
ENST00000422285.6:c.760-27C>T ENSP00000394382.2:n.760-27C>T
ENST00000481733.1:n.188-27C>T
ENST00000540249.5:c.667-27C>T ENSP00000440761.1:n.667-27C>T
ENST00000545074.5:c.781-27C>T ENSP00000438550.1:n.781-27C>T
NM_000284.3:c.760-27C>T NP_000275.1:n.760-27C>T
NM_001173454.1:c.874-27C>T NP_001166925.1:n.874-27C>T
NM_001173455.1:c.781-27C>T NP_001166926.1:n.781-27C>T
NM_001173456.1:c.667-27C>T NP_001166927.1:n.667-27C>T
XM_011545531.1:c.895-27C>T XP_011543833.1:n.895-27C>T
XM_011545532.1:c.802-27C>T XP_011543834.1:n.802-27C>T
XM_017029574.2:c.781-27C>T XP_016885063.1:n.781-27C>T
NM_000284.4:c.760-27C>T MANE Select NP_000275.1:n.760-27C>T
NM_001173454.2:c.874-27C>T NP_001166925.1:n.874-27C>T
NM_001173455.2:c.781-27C>T NP_001166926.1:n.781-27C>T
NM_001173456.2:c.667-27C>T NP_001166927.1:n.667-27C>T