Canonical Allele Identifier: CA873738961

Gene: PDHA1

Linked Data

• dbSNP Id: rs1464274881
• MyVariant Identifiers: chrX:g.19373438A>G (hg19) ; chrX:g.19355320A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355320A>G , CM000685.2:g.19355320A>G	GRCh38
NC_000023.10:g.19373438A>G , CM000685.1:g.19373438A>G	GRCh37
NC_000023.9:g.19283359A>G	NCBI36
NG_016781.1:g.16428A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.625-29A>G	ENSP00000348062.6:n.625-29A>G
ENST00000379805.4:c.*296-29A>G	ENSP00000369133.3:n.*296-29A>G
ENST00000417819.6:c.688-29A>G	ENSP00000404616.2:n.688-29A>G
ENST00000423505.6:c.718-29A>G	ENSP00000406473.2:n.718-29A>G
ENST00000481733.2:n.370A>G
ENST00000696704.1:c.419-29A>G	ENSP00000512823.1:n.419-29A>G
ENST00000696705.1:c.*59-29A>G	ENSP00000512824.1:n.*59-29A>G
ENST00000422285.7:c.604-29A>G MANE Select	ENSP00000394382.2:n.604-29A>G
ENST00000379806.9:c.718-29A>G	ENSP00000369134.5:n.718-29A>G
ENST00000422285.6:c.604-29A>G	ENSP00000394382.2:n.604-29A>G
ENST00000479146.1:n.439-29A>G
ENST00000481733.1:n.3A>G
ENST00000540249.5:c.511-29A>G	ENSP00000440761.1:n.511-29A>G
ENST00000545074.5:c.625-29A>G	ENSP00000438550.1:n.625-29A>G
NM_000284.3:c.604-29A>G	NP_000275.1:n.604-29A>G
NM_001173454.1:c.718-29A>G	NP_001166925.1:n.718-29A>G
NM_001173455.1:c.625-29A>G	NP_001166926.1:n.625-29A>G
NM_001173456.1:c.511-29A>G	NP_001166927.1:n.511-29A>G
XM_011545531.1:c.739-29A>G	XP_011543833.1:n.739-29A>G
XM_011545532.1:c.646-29A>G	XP_011543834.1:n.646-29A>G
XM_017029574.2:c.625-29A>G	XP_016885063.1:n.625-29A>G
NM_000284.4:c.604-29A>G MANE Select	NP_000275.1:n.604-29A>G
NM_001173454.2:c.718-29A>G	NP_001166925.1:n.718-29A>G
NM_001173455.2:c.625-29A>G	NP_001166926.1:n.625-29A>G
NM_001173456.2:c.511-29A>G	NP_001166927.1:n.511-29A>G