Canonical Allele Identifier: CA515485214
Gene: PDHA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.19368066T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19349948T>G , CM000685.2:g.19349948T>G GRCh38
NC_000023.10:g.19368066T>G , CM000685.1:g.19368066T>G GRCh37
NC_000023.9:g.19277987T>G NCBI36
NG_016781.1:g.11056T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.129T>G ENSP00000348062.6:p.Leu43=
ENST00000379805.4:c.129T>G ENSP00000369133.3:p.Leu43=
ENST00000417819.6:c.213T>G ENSP00000404616.2:p.Leu71=
ENST00000423505.6:c.243T>G ENSP00000406473.2:p.Leu81=
ENST00000696704.1:c.129T>G ENSP00000512823.1:p.Leu43=
ENST00000696705.1:c.129T>G ENSP00000512824.1:p.Leu43=
ENST00000422285.7:c.129T>G MANE Select ENSP00000394382.2:p.Leu43=
ENST00000355808.9:c.129T>G ENSP00000348062.5:p.Leu43=
ENST00000379805.3:c.129T>G ENSP00000369133.3:p.Leu43=
ENST00000379806.9:c.243T>G ENSP00000369134.5:p.Leu81=
ENST00000417819.5:c.213T>G ENSP00000404616.1:p.Leu71=
ENST00000422285.6:c.129T>G ENSP00000394382.2:p.Leu43=
ENST00000423505.5:c.243T>G ENSP00000406473.1:p.Leu81=
ENST00000492364.1:n.231T>G
ENST00000540249.5:c.129T>G ENSP00000440761.1:p.Leu43=
ENST00000545074.5:c.129T>G ENSP00000438550.1:p.Leu43=
NM_000284.3:c.129T>G NP_000275.1:p.Leu43=
NM_001173454.1:c.243T>G NP_001166925.1:p.Leu81=
NM_001173455.1:c.129T>G NP_001166926.1:p.Leu43=
NM_001173456.1:c.129T>G NP_001166927.1:p.Leu43=
XM_011545531.1:c.243T>G XP_011543833.1:p.Leu81=
XM_011545532.1:c.243T>G XP_011543834.1:p.Leu81=
XM_017029574.2:c.243T>G XP_016885063.1:p.Leu81=
NM_000284.4:c.129T>G MANE Select NP_000275.1:p.Leu43=
NM_001173454.2:c.243T>G NP_001166925.1:p.Leu81=
NM_001173455.2:c.129T>G NP_001166926.1:p.Leu43=
NM_001173456.2:c.129T>G NP_001166927.1:p.Leu43=