Canonical Allele Identifier: CA2693251509
Gene: PDHA1 HGNC NCBI

Linked Data

gnomAD v4: X-19359917-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359917C>T , CM000685.2:g.19359917C>T GRCh38
NC_000023.10:g.19378035C>T , CM000685.1:g.19378035C>T GRCh37
NC_000023.9:g.19287956C>T NCBI36
NG_016781.1:g.21025C>T
NG_021184.1:g.160345G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*264C>T ENSP00000348062.6:n.*264C>T
ENST00000423505.6:c.*264C>T ENSP00000406473.2:n.*264C>T
ENST00000696704.1:c.*769C>T ENSP00000512823.1:n.*769C>T
ENST00000696705.1:c.*892C>T ENSP00000512824.1:n.*892C>T
ENST00000422285.7:c.*264C>T MANE Select ENSP00000394382.2:n.*264C>T
ENST00000379806.9:c.*264C>T ENSP00000369134.5:n.*264C>T
ENST00000422285.6:c.*264C>T ENSP00000394382.2:n.*264C>T
ENST00000540249.5:c.*264C>T ENSP00000440761.1:n.*264C>T
ENST00000545074.5:c.*264C>T ENSP00000438550.1:n.*264C>T
NM_000284.3:c.*264C>T NP_000275.1:n.*264C>T
NM_001173454.1:c.*264C>T NP_001166925.1:n.*264C>T
NM_001173455.1:c.*264C>T NP_001166926.1:n.*264C>T
NM_001173456.1:c.*264C>T NP_001166927.1:n.*264C>T
XM_011545531.1:c.*264C>T XP_011543833.1:n.*264C>T
XM_011545532.1:c.*264C>T XP_011543834.1:n.*264C>T
NM_000284.4:c.*264C>T MANE Select NP_000275.1:n.*264C>T
NM_001173454.2:c.*264C>T NP_001166925.1:n.*264C>T
NM_001173455.2:c.*264C>T NP_001166926.1:n.*264C>T
NM_001173456.2:c.*264C>T NP_001166927.1:n.*264C>T