Canonical Allele Identifier: CA515485987

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19373475A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355357A>C , CM000685.2:g.19355357A>C	GRCh38
NC_000023.10:g.19373475A>C , CM000685.1:g.19373475A>C	GRCh37
NC_000023.9:g.19283396A>C	NCBI36
NG_016781.1:g.16465A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.633A>C	ENSP00000348062.6:p.Ile211=
ENST00000379805.4:c.*304A>C	ENSP00000369133.3:n.*304A>C
ENST00000417819.6:c.696A>C	ENSP00000404616.2:p.Ile232=
ENST00000423505.6:c.726A>C	ENSP00000406473.2:p.Ile242=
ENST00000481733.2:n.407A>C
ENST00000696704.1:c.427A>C	ENSP00000512823.1:p.Ile143Leu
ENST00000696705.1:c.*67A>C	ENSP00000512824.1:n.*67A>C
ENST00000422285.7:c.612A>C MANE Select	ENSP00000394382.2:p.Ile204=
ENST00000379806.9:c.726A>C	ENSP00000369134.5:p.Ile242=
ENST00000422285.6:c.612A>C	ENSP00000394382.2:p.Ile204=
ENST00000479146.1:n.447A>C
ENST00000481733.1:n.40A>C
ENST00000540249.5:c.519A>C	ENSP00000440761.1:p.Ile173=
ENST00000545074.5:c.633A>C	ENSP00000438550.1:p.Ile211=
NM_000284.3:c.612A>C	NP_000275.1:p.Ile204=
NM_001173454.1:c.726A>C	NP_001166925.1:p.Ile242=
NM_001173455.1:c.633A>C	NP_001166926.1:p.Ile211=
NM_001173456.1:c.519A>C	NP_001166927.1:p.Ile173=
XM_011545531.1:c.747A>C	XP_011543833.1:p.Ile249=
XM_011545532.1:c.654A>C	XP_011543834.1:p.Ile218=
XM_017029574.2:c.633A>C	XP_016885063.1:p.Ile211=
NM_000284.4:c.612A>C MANE Select	NP_000275.1:p.Ile204=
NM_001173454.2:c.726A>C	NP_001166925.1:p.Ile242=
NM_001173455.2:c.633A>C	NP_001166926.1:p.Ile211=
NM_001173456.2:c.519A>C	NP_001166927.1:p.Ile173=