Canonical Allele Identifier: CA515486491

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377762A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359644A>G , CM000685.2:g.19359644A>G	GRCh38
NC_000023.10:g.19377762A>G , CM000685.1:g.19377762A>G	GRCh37
NC_000023.9:g.19287683A>G	NCBI36
NG_016781.1:g.20752A>G
NG_021184.1:g.160618T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.1185A>G	ENSP00000348062.6:p.Ser395=
ENST00000379805.4:c.*856A>G	ENSP00000369133.3:n.*856A>G
ENST00000417819.6:c.1248A>G	ENSP00000404616.2:p.Ser416=
ENST00000423505.6:c.1278A>G	ENSP00000406473.2:p.Ser426=
ENST00000481733.2:n.959A>G
ENST00000696704.1:c.*496A>G	ENSP00000512823.1:n.*496A>G
ENST00000696705.1:c.*619A>G	ENSP00000512824.1:n.*619A>G
ENST00000422285.7:c.1164A>G MANE Select	ENSP00000394382.2:p.Ser388=
ENST00000379804.1:c.321A>G	ENSP00000369132.1:p.Ser107=
ENST00000379806.9:c.1278A>G	ENSP00000369134.5:p.Ser426=
ENST00000422285.6:c.1164A>G	ENSP00000394382.2:p.Ser388=
ENST00000478795.1:n.603A>G
ENST00000540249.5:c.1071A>G	ENSP00000440761.1:p.Ser357=
ENST00000545074.5:c.1185A>G	ENSP00000438550.1:p.Ser395=
NM_000284.3:c.1164A>G	NP_000275.1:p.Ser388=
NM_001173454.1:c.1278A>G	NP_001166925.1:p.Ser426=
NM_001173455.1:c.1185A>G	NP_001166926.1:p.Ser395=
NM_001173456.1:c.1071A>G	NP_001166927.1:p.Ser357=
XM_011545531.1:c.1299A>G	XP_011543833.1:p.Ser433=
XM_011545532.1:c.1206A>G	XP_011543834.1:p.Ser402=
XM_017029574.2:c.1185A>G	XP_016885063.1:p.Ser395=
NM_000284.4:c.1164A>G MANE Select	NP_000275.1:p.Ser388=
NM_001173454.2:c.1278A>G	NP_001166925.1:p.Ser426=
NM_001173455.2:c.1185A>G	NP_001166926.1:p.Ser395=
NM_001173456.2:c.1071A>G	NP_001166927.1:p.Ser357=