Canonical Allele Identifier: CA515486423

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19377645T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359527T>G , CM000685.2:g.19359527T>G	GRCh38
NC_000023.10:g.19377645T>G , CM000685.1:g.19377645T>G	GRCh37
NC_000023.9:g.19287566T>G	NCBI36
NG_016781.1:g.20635T>G
NG_021184.1:g.160735A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.1068T>G	ENSP00000348062.6:p.Ala356=
ENST00000379805.4:c.*739T>G	ENSP00000369133.3:n.*739T>G
ENST00000417819.6:c.1131T>G	ENSP00000404616.2:p.Ala377=
ENST00000423505.6:c.1161T>G	ENSP00000406473.2:p.Ala387=
ENST00000481733.2:n.842T>G
ENST00000696704.1:c.*379T>G	ENSP00000512823.1:n.*379T>G
ENST00000696705.1:c.*502T>G	ENSP00000512824.1:n.*502T>G
ENST00000422285.7:c.1047T>G MANE Select	ENSP00000394382.2:p.Ala349=
ENST00000379804.1:c.204T>G	ENSP00000369132.1:p.Ala68=
ENST00000379806.9:c.1161T>G	ENSP00000369134.5:p.Ala387=
ENST00000422285.6:c.1047T>G	ENSP00000394382.2:p.Ala349=
ENST00000478795.1:n.486T>G
ENST00000540249.5:c.954T>G	ENSP00000440761.1:p.Ala318=
ENST00000545074.5:c.1068T>G	ENSP00000438550.1:p.Ala356=
NM_000284.3:c.1047T>G	NP_000275.1:p.Ala349=
NM_001173454.1:c.1161T>G	NP_001166925.1:p.Ala387=
NM_001173455.1:c.1068T>G	NP_001166926.1:p.Ala356=
NM_001173456.1:c.954T>G	NP_001166927.1:p.Ala318=
XM_011545531.1:c.1182T>G	XP_011543833.1:p.Ala394=
XM_011545532.1:c.1089T>G	XP_011543834.1:p.Ala363=
XM_017029574.2:c.1068T>G	XP_016885063.1:p.Ala356=
NM_000284.4:c.1047T>G MANE Select	NP_000275.1:p.Ala349=
NM_001173454.2:c.1161T>G	NP_001166925.1:p.Ala387=
NM_001173455.2:c.1068T>G	NP_001166926.1:p.Ala356=
NM_001173456.2:c.954T>G	NP_001166927.1:p.Ala318=