Canonical Allele Identifier: CA2693250976

Gene: PDHA1

Linked Data

• gnomAD v4: X-19357827-T-TTCATGTACGCAG

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357829_19357840dup , CM000685.2:g.19357829_19357840dup	GRCh38
NC_000023.10:g.19375947_19375958dup , CM000685.1:g.19375947_19375958dup	GRCh37
NC_000023.9:g.19285868_19285879dup	NCBI36
NG_016781.1:g.18937_18948dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.920+110_920+121dup	ENSP00000348062.6:n.920+110_920+121dup
ENST00000379805.4:c.*591+110_*591+121dup	ENSP00000369133.3:n.*591+110_*591+121dup
ENST00000417819.6:c.983+110_983+121dup	ENSP00000404616.2:n.983+110_983+121dup
ENST00000423505.6:c.1013+110_1013+121dup	ENSP00000406473.2:n.1013+110_1013+121dup
ENST00000481733.2:n.694+110_694+121dup
ENST00000696704.1:c.*231+110_*231+121dup	ENSP00000512823.1:n.*231+110_*231+121dup
ENST00000696705.1:c.*354+110_*354+121dup	ENSP00000512824.1:n.*354+110_*354+121dup
ENST00000422285.7:c.899+110_899+121dup MANE Select	ENSP00000394382.2:n.899+110_899+121dup
ENST00000379804.1:c.56+110_56+121dup	ENSP00000369132.1:n.56+110_56+121dup
ENST00000379806.9:c.1013+110_1013+121dup	ENSP00000369134.5:n.1013+110_1013+121dup
ENST00000422285.6:c.899+110_899+121dup	ENSP00000394382.2:n.899+110_899+121dup
ENST00000478795.1:n.338+110_338+121dup
ENST00000481733.1:n.327+110_327+121dup
ENST00000540249.5:c.806+110_806+121dup	ENSP00000440761.1:n.806+110_806+121dup
ENST00000545074.5:c.920+110_920+121dup	ENSP00000438550.1:n.920+110_920+121dup
NM_000284.3:c.899+110_899+121dup	NP_000275.1:n.899+110_899+121dup
NM_001173454.1:c.1013+110_1013+121dup	NP_001166925.1:n.1013+110_1013+121dup
NM_001173455.1:c.920+110_920+121dup	NP_001166926.1:n.920+110_920+121dup
NM_001173456.1:c.806+110_806+121dup	NP_001166927.1:n.806+110_806+121dup
XM_011545531.1:c.1034+110_1034+121dup	XP_011543833.1:n.1034+110_1034+121dup
XM_011545532.1:c.941+110_941+121dup	XP_011543834.1:n.941+110_941+121dup
XM_017029574.2:c.920+110_920+121dup	XP_016885063.1:n.920+110_920+121dup
NM_000284.4:c.899+110_899+121dup MANE Select	NP_000275.1:n.899+110_899+121dup
NM_001173454.2:c.1013+110_1013+121dup	NP_001166925.1:n.1013+110_1013+121dup
NM_001173455.2:c.920+110_920+121dup	NP_001166926.1:n.920+110_920+121dup
NM_001173456.2:c.806+110_806+121dup	NP_001166927.1:n.806+110_806+121dup