Canonical Allele Identifier: CA515485870

Gene: PDHA1

Linked Data

• MyVariant Identifiers: chrX:g.19371219T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19353101T>G , CM000685.2:g.19353101T>G	GRCh38
NC_000023.10:g.19371219T>G , CM000685.1:g.19371219T>G	GRCh37
NC_000023.9:g.19281140T>G	NCBI36
NG_016781.1:g.14209T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.459T>G	ENSP00000348062.6:p.Ala153=
ENST00000379805.4:c.438T>G	ENSP00000369133.3:p.Ala146=
ENST00000417819.6:c.522T>G	ENSP00000404616.2:p.Ala174=
ENST00000423505.6:c.552T>G	ENSP00000406473.2:p.Ala184=
ENST00000696704.1:c.418+1694T>G	ENSP00000512823.1:n.418+1694T>G
ENST00000696705.1:c.419-1390T>G	ENSP00000512824.1:n.419-1390T>G
ENST00000422285.7:c.438T>G MANE Select	ENSP00000394382.2:p.Ala146=
ENST00000355808.9:c.459T>G	ENSP00000348062.5:p.Ala153=
ENST00000379805.3:c.438T>G	ENSP00000369133.3:p.Ala146=
ENST00000379806.9:c.552T>G	ENSP00000369134.5:p.Ala184=
ENST00000422285.6:c.438T>G	ENSP00000394382.2:p.Ala146=
ENST00000423505.5:c.552T>G	ENSP00000406473.1:p.Ala184=
ENST00000479146.1:n.273T>G
ENST00000540249.5:c.438T>G	ENSP00000440761.1:p.Ala146=
ENST00000545074.5:c.459T>G	ENSP00000438550.1:p.Ala153=
NM_000284.3:c.438T>G	NP_000275.1:p.Ala146=
NM_001173454.1:c.552T>G	NP_001166925.1:p.Ala184=
NM_001173455.1:c.459T>G	NP_001166926.1:p.Ala153=
NM_001173456.1:c.438T>G	NP_001166927.1:p.Ala146=
XM_011545531.1:c.573T>G	XP_011543833.1:p.Ala191=
XM_011545532.1:c.573T>G	XP_011543834.1:p.Ala191=
XM_017029574.2:c.552T>G	XP_016885063.1:p.Ala184=
NM_000284.4:c.438T>G MANE Select	NP_000275.1:p.Ala146=
NM_001173454.2:c.552T>G	NP_001166925.1:p.Ala184=
NM_001173455.2:c.459T>G	NP_001166926.1:p.Ala153=
NM_001173456.2:c.438T>G	NP_001166927.1:p.Ala146=