Canonical Allele Identifier: CA2418224727

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357946_19357948delinsGAA , CM000685.2:g.19357946_19357948delinsGAA	GRCh38
NC_000023.10:g.19376064_19376066delinsGAA , CM000685.1:g.19376064_19376066delinsGAA	GRCh37
NC_000023.9:g.19285985_19285987delinsGAA	NCBI36
NG_016781.1:g.19054_19056delinsGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.920+227_920+229delinsGAA	ENSP00000348062.6:n.920+227_920+229delinsGAA
ENST00000379805.4:c.*591+227_*591+229delinsGAA	ENSP00000369133.3:n.*591+227_*591+229delinsGAA
ENST00000417819.6:c.983+227_983+229delinsGAA	ENSP00000404616.2:n.983+227_983+229delinsGAA
ENST00000423505.6:c.1013+227_1013+229delinsGAA	ENSP00000406473.2:n.1013+227_1013+229delinsGAA
ENST00000481733.2:n.694+227_694+229delinsGAA
ENST00000696704.1:c.*231+227_*231+229delinsGAA	ENSP00000512823.1:n.*231+227_*231+229delinsGAA
ENST00000696705.1:c.*354+227_*354+229delinsGAA	ENSP00000512824.1:n.*354+227_*354+229delinsGAA
ENST00000422285.7:c.899+227_899+229delinsGAA MANE Select	ENSP00000394382.2:n.899+227_899+229delinsGAA
ENST00000379804.1:c.56+227_56+229delinsGAA	ENSP00000369132.1:n.56+227_56+229delinsGAA
ENST00000379806.9:c.1013+227_1013+229delinsGAA	ENSP00000369134.5:n.1013+227_1013+229delinsGAA
ENST00000422285.6:c.899+227_899+229delinsGAA	ENSP00000394382.2:n.899+227_899+229delinsGAA
ENST00000478795.1:n.338+227_338+229delinsGAA
ENST00000481733.1:n.327+227_327+229delinsGAA
ENST00000540249.5:c.806+227_806+229delinsGAA	ENSP00000440761.1:n.806+227_806+229delinsGAA
ENST00000545074.5:c.920+227_920+229delinsGAA	ENSP00000438550.1:n.920+227_920+229delinsGAA
NM_000284.3:c.899+227_899+229delinsGAA	NP_000275.1:n.899+227_899+229delinsGAA
NM_001173454.1:c.1013+227_1013+229delinsGAA	NP_001166925.1:n.1013+227_1013+229delinsGAA
NM_001173455.1:c.920+227_920+229delinsGAA	NP_001166926.1:n.920+227_920+229delinsGAA
NM_001173456.1:c.806+227_806+229delinsGAA	NP_001166927.1:n.806+227_806+229delinsGAA
XM_011545531.1:c.1034+227_1034+229delinsGAA	XP_011543833.1:n.1034+227_1034+229delinsGAA
XM_011545532.1:c.941+227_941+229delinsGAA	XP_011543834.1:n.941+227_941+229delinsGAA
XM_017029574.2:c.920+227_920+229delinsGAA	XP_016885063.1:n.920+227_920+229delinsGAA
NM_000284.4:c.899+227_899+229delinsGAA MANE Select	NP_000275.1:n.899+227_899+229delinsGAA
NM_001173454.2:c.1013+227_1013+229delinsGAA	NP_001166925.1:n.1013+227_1013+229delinsGAA
NM_001173455.2:c.920+227_920+229delinsGAA	NP_001166926.1:n.920+227_920+229delinsGAA
NM_001173456.2:c.806+227_806+229delinsGAA	NP_001166927.1:n.806+227_806+229delinsGAA