Canonical Allele Identifier: CA2541314439

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357858del , CM000685.2:g.19357858del	GRCh38
NC_000023.10:g.19375976del , CM000685.1:g.19375976del	GRCh37
NC_000023.9:g.19285897del	NCBI36
NG_016781.1:g.18966del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.920+139del	ENSP00000348062.6:n.920+139del
ENST00000379805.4:c.*591+139del	ENSP00000369133.3:n.*591+139del
ENST00000417819.6:c.983+139del	ENSP00000404616.2:n.983+139del
ENST00000423505.6:c.1013+139del	ENSP00000406473.2:n.1013+139del
ENST00000481733.2:n.694+139del
ENST00000696704.1:c.*231+139del	ENSP00000512823.1:n.*231+139del
ENST00000696705.1:c.*354+139del	ENSP00000512824.1:n.*354+139del
ENST00000422285.7:c.899+139del MANE Select	ENSP00000394382.2:n.899+139del
ENST00000379804.1:c.56+139del	ENSP00000369132.1:n.56+139del
ENST00000379806.9:c.1013+139del	ENSP00000369134.5:n.1013+139del
ENST00000422285.6:c.899+139del	ENSP00000394382.2:n.899+139del
ENST00000478795.1:n.338+139del
ENST00000481733.1:n.327+139del
ENST00000540249.5:c.806+139del	ENSP00000440761.1:n.806+139del
ENST00000545074.5:c.920+139del	ENSP00000438550.1:n.920+139del
NM_000284.3:c.899+139del	NP_000275.1:n.899+139del
NM_001173454.1:c.1013+139del	NP_001166925.1:n.1013+139del
NM_001173455.1:c.920+139del	NP_001166926.1:n.920+139del
NM_001173456.1:c.806+139del	NP_001166927.1:n.806+139del
XM_011545531.1:c.1034+139del	XP_011543833.1:n.1034+139del
XM_011545532.1:c.941+139del	XP_011543834.1:n.941+139del
XM_017029574.2:c.920+139del	XP_016885063.1:n.920+139del
NM_000284.4:c.899+139del MANE Select	NP_000275.1:n.899+139del
NM_001173454.2:c.1013+139del	NP_001166925.1:n.1013+139del
NM_001173455.2:c.920+139del	NP_001166926.1:n.920+139del
NM_001173456.2:c.806+139del	NP_001166927.1:n.806+139del