Canonical Allele Identifier: CA515485516
Gene: PDHA1 HGNC NCBI

Linked Data

gnomAD v4: X-19351301-G-A
MyVariant Identifiers: chrX:g.19369419G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19351301G>A , CM000685.2:g.19351301G>A GRCh38
NC_000023.10:g.19369419G>A , CM000685.1:g.19369419G>A GRCh37
NC_000023.9:g.19279340G>A NCBI36
NG_016781.1:g.12409G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.333G>A ENSP00000348062.6:p.Leu111=
ENST00000379805.4:c.312G>A ENSP00000369133.3:p.Leu104=
ENST00000417819.6:c.396G>A ENSP00000404616.2:p.Leu132=
ENST00000423505.6:c.426G>A ENSP00000406473.2:p.Leu142=
ENST00000696704.1:c.312G>A ENSP00000512823.1:p.Leu104=
ENST00000696705.1:c.312G>A ENSP00000512824.1:p.Leu104=
ENST00000422285.7:c.312G>A MANE Select ENSP00000394382.2:p.Leu104=
ENST00000355808.9:c.333G>A ENSP00000348062.5:p.Leu111=
ENST00000379805.3:c.312G>A ENSP00000369133.3:p.Leu104=
ENST00000379806.9:c.426G>A ENSP00000369134.5:p.Leu142=
ENST00000422285.6:c.312G>A ENSP00000394382.2:p.Leu104=
ENST00000423505.5:c.426G>A ENSP00000406473.1:p.Leu142=
ENST00000492364.1:n.414G>A
ENST00000540249.5:c.312G>A ENSP00000440761.1:p.Leu104=
ENST00000545074.5:c.333G>A ENSP00000438550.1:p.Leu111=
NM_000284.3:c.312G>A NP_000275.1:p.Leu104=
NM_001173454.1:c.426G>A NP_001166925.1:p.Leu142=
NM_001173455.1:c.333G>A NP_001166926.1:p.Leu111=
NM_001173456.1:c.312G>A NP_001166927.1:p.Leu104=
XM_011545531.1:c.447G>A XP_011543833.1:p.Leu149=
XM_011545532.1:c.447G>A XP_011543834.1:p.Leu149=
XM_017029574.2:c.426G>A XP_016885063.1:p.Leu142=
NM_000284.4:c.312G>A MANE Select NP_000275.1:p.Leu104=
NM_001173454.2:c.426G>A NP_001166925.1:p.Leu142=
NM_001173455.2:c.333G>A NP_001166926.1:p.Leu111=
NM_001173456.2:c.312G>A NP_001166927.1:p.Leu104=