Canonical Allele Identifier: CA412394686

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373614G>T (hg19) ; chrX:g.19355496G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355496G>T , CM000685.2:g.19355496G>T	GRCh38
NC_000023.10:g.19373614G>T , CM000685.1:g.19373614G>T	GRCh37
NC_000023.9:g.19283535G>T	NCBI36
NG_016781.1:g.16604G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.772G>T	ENSP00000348062.6:p.Gly258Trp
ENST00000379805.4:c.*443G>T	ENSP00000369133.3:n.*443G>T
ENST00000417819.6:c.835G>T	ENSP00000404616.2:p.Gly279Trp
ENST00000423505.6:c.865G>T	ENSP00000406473.2:p.Gly289Trp
ENST00000481733.2:n.546G>T
ENST00000696704.1:c.*83G>T	ENSP00000512823.1:n.*83G>T
ENST00000696705.1:c.*206G>T	ENSP00000512824.1:n.*206G>T
ENST00000422285.7:c.751G>T MANE Select	ENSP00000394382.2:p.Gly251Trp
ENST00000379806.9:c.865G>T	ENSP00000369134.5:p.Gly289Trp
ENST00000422285.6:c.751G>T	ENSP00000394382.2:p.Gly251Trp
ENST00000481733.1:n.179G>T
ENST00000540249.5:c.658G>T	ENSP00000440761.1:p.Gly220Trp
ENST00000545074.5:c.772G>T	ENSP00000438550.1:p.Gly258Trp
NM_000284.3:c.751G>T	NP_000275.1:p.Gly251Trp
NM_001173454.1:c.865G>T	NP_001166925.1:p.Gly289Trp
NM_001173455.1:c.772G>T	NP_001166926.1:p.Gly258Trp
NM_001173456.1:c.658G>T	NP_001166927.1:p.Gly220Trp
XM_011545531.1:c.886G>T	XP_011543833.1:p.Gly296Trp
XM_011545532.1:c.793G>T	XP_011543834.1:p.Gly265Trp
XM_017029574.2:c.772G>T	XP_016885063.1:p.Gly258Trp
NM_000284.4:c.751G>T MANE Select	NP_000275.1:p.Gly251Trp
NM_001173454.2:c.865G>T	NP_001166925.1:p.Gly289Trp
NM_001173455.2:c.772G>T	NP_001166926.1:p.Gly258Trp
NM_001173456.2:c.658G>T	NP_001166927.1:p.Gly220Trp