Canonical Allele Identifier: CA10363021
Gene: PDHA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1599813
ClinVar RCV Id: RCV002116179
dbSNP Id: rs776535833
gnomAD v2: X-19369388-C-T
gnomAD v3: X-19351270-C-T
gnomAD v4: X-19351270-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19351270C>T , CM000685.2:g.19351270C>T GRCh38
NC_000023.10:g.19369388C>T , CM000685.1:g.19369388C>T GRCh37
NC_000023.9:g.19279309C>T NCBI36
NG_016781.1:g.12378C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.302C>T ENSP00000348062.6:p.Pro101Leu
ENST00000379805.4:c.292-11C>T ENSP00000369133.3:n.292-11C>T
ENST00000417819.6:c.376-11C>T ENSP00000404616.2:n.376-11C>T
ENST00000423505.6:c.406-11C>T ENSP00000406473.2:n.406-11C>T
ENST00000696704.1:c.292-11C>T ENSP00000512823.1:n.292-11C>T
ENST00000696705.1:c.292-11C>T ENSP00000512824.1:n.292-11C>T
ENST00000422285.7:c.292-11C>T MANE Select ENSP00000394382.2:n.292-11C>T
ENST00000355808.9:c.302C>T ENSP00000348062.5:p.Pro101Leu
ENST00000379805.3:c.292-11C>T ENSP00000369133.3:n.292-11C>T
ENST00000379806.9:c.406-11C>T ENSP00000369134.5:n.406-11C>T
ENST00000422285.6:c.292-11C>T ENSP00000394382.2:n.292-11C>T
ENST00000423505.5:c.406-11C>T ENSP00000406473.1:n.406-11C>T
ENST00000492364.1:n.394-11C>T
ENST00000540249.5:c.292-11C>T ENSP00000440761.1:n.292-11C>T
ENST00000545074.5:c.302C>T ENSP00000438550.1:p.Pro101Leu
NM_000284.3:c.292-11C>T NP_000275.1:n.292-11C>T
NM_001173454.1:c.406-11C>T NP_001166925.1:n.406-11C>T
NM_001173455.1:c.302C>T NP_001166926.1:p.Pro101Leu
NM_001173456.1:c.292-11C>T NP_001166927.1:n.292-11C>T
XM_011545531.1:c.416C>T XP_011543833.1:p.Pro139Leu
XM_011545532.1:c.416C>T XP_011543834.1:p.Pro139Leu
XM_017029574.2:c.406-11C>T XP_016885063.1:n.406-11C>T
NM_000284.4:c.292-11C>T MANE Select NP_000275.1:n.292-11C>T
NM_001173454.2:c.406-11C>T NP_001166925.1:n.406-11C>T
NM_001173455.2:c.302C>T NP_001166926.1:p.Pro101Leu
NM_001173456.2:c.292-11C>T NP_001166927.1:n.292-11C>T