Canonical Allele Identifier: CA412396147

Gene: PDHA1

Linked Data

• gnomAD v4: X-19358956-A-G
• MyVariant Identifiers: chrX:g.19377074A>G (hg19) ; chrX:g.19358956A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358956A>G , CM000685.2:g.19358956A>G	GRCh38
NC_000023.10:g.19377074A>G , CM000685.1:g.19377074A>G	GRCh37
NC_000023.9:g.19286995A>G	NCBI36
NG_016781.1:g.20064A>G
NG_021184.1:g.161306T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.961A>G	ENSP00000348062.6:p.Ser321Gly
ENST00000379805.4:c.*632A>G	ENSP00000369133.3:n.*632A>G
ENST00000417819.6:c.1024A>G	ENSP00000404616.2:p.Ser342Gly
ENST00000423505.6:c.1054A>G	ENSP00000406473.2:p.Ser352Gly
ENST00000481733.2:n.735A>G
ENST00000696704.1:c.*272A>G	ENSP00000512823.1:n.*272A>G
ENST00000696705.1:c.*395A>G	ENSP00000512824.1:n.*395A>G
ENST00000422285.7:c.940A>G MANE Select	ENSP00000394382.2:p.Ser314Gly
ENST00000379804.1:c.97A>G	ENSP00000369132.1:p.Ser33Gly
ENST00000379806.9:c.1054A>G	ENSP00000369134.5:p.Ser352Gly
ENST00000422285.6:c.940A>G	ENSP00000394382.2:p.Ser314Gly
ENST00000478795.1:n.379A>G
ENST00000481733.1:n.368A>G
ENST00000540249.5:c.847A>G	ENSP00000440761.1:p.Ser283Gly
ENST00000545074.5:c.961A>G	ENSP00000438550.1:p.Ser321Gly
NM_000284.3:c.940A>G	NP_000275.1:p.Ser314Gly
NM_001173454.1:c.1054A>G	NP_001166925.1:p.Ser352Gly
NM_001173455.1:c.961A>G	NP_001166926.1:p.Ser321Gly
NM_001173456.1:c.847A>G	NP_001166927.1:p.Ser283Gly
XM_011545531.1:c.1075A>G	XP_011543833.1:p.Ser359Gly
XM_011545532.1:c.982A>G	XP_011543834.1:p.Ser328Gly
XM_017029574.2:c.961A>G	XP_016885063.1:p.Ser321Gly
NM_000284.4:c.940A>G MANE Select	NP_000275.1:p.Ser314Gly
NM_001173454.2:c.1054A>G	NP_001166925.1:p.Ser352Gly
NM_001173455.2:c.961A>G	NP_001166926.1:p.Ser321Gly
NM_001173456.2:c.847A>G	NP_001166927.1:p.Ser283Gly