Canonical Allele Identifier: CA2693251420
Gene: PDHA1 HGNC NCBI

Linked Data

gnomAD v4: X-19359777-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359777G>A , CM000685.2:g.19359777G>A GRCh38
NC_000023.10:g.19377895G>A , CM000685.1:g.19377895G>A GRCh37
NC_000023.9:g.19287816G>A NCBI36
NG_016781.1:g.20885G>A
NG_021184.1:g.160485C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*124G>A ENSP00000348062.6:n.*124G>A
ENST00000379805.4:c.*989G>A ENSP00000369133.3:n.*989G>A
ENST00000417819.6:c.*124G>A ENSP00000404616.2:n.*124G>A
ENST00000423505.6:c.*124G>A ENSP00000406473.2:n.*124G>A
ENST00000481733.2:n.1092G>A
ENST00000696704.1:c.*629G>A ENSP00000512823.1:n.*629G>A
ENST00000696705.1:c.*752G>A ENSP00000512824.1:n.*752G>A
ENST00000422285.7:c.*124G>A MANE Select ENSP00000394382.2:n.*124G>A
ENST00000379804.1:c.*124G>A ENSP00000369132.1:n.*124G>A
ENST00000379806.9:c.*124G>A ENSP00000369134.5:n.*124G>A
ENST00000422285.6:c.*124G>A ENSP00000394382.2:n.*124G>A
ENST00000478795.1:n.736G>A
ENST00000540249.5:c.*124G>A ENSP00000440761.1:n.*124G>A
ENST00000545074.5:c.*124G>A ENSP00000438550.1:n.*124G>A
NM_000284.3:c.*124G>A NP_000275.1:n.*124G>A
NM_001173454.1:c.*124G>A NP_001166925.1:n.*124G>A
NM_001173455.1:c.*124G>A NP_001166926.1:n.*124G>A
NM_001173456.1:c.*124G>A NP_001166927.1:n.*124G>A
XM_011545531.1:c.*124G>A XP_011543833.1:n.*124G>A
XM_011545532.1:c.*124G>A XP_011543834.1:n.*124G>A
XM_017029574.2:c.*124G>A XP_016885063.1:n.*124G>A
NM_000284.4:c.*124G>A MANE Select NP_000275.1:n.*124G>A
NM_001173454.2:c.*124G>A NP_001166925.1:n.*124G>A
NM_001173455.2:c.*124G>A NP_001166926.1:n.*124G>A
NM_001173456.2:c.*124G>A NP_001166927.1:n.*124G>A