Canonical Allele Identifier: CA2418222069

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19351223_19351225delinsGTT , CM000685.2:g.19351223_19351225delinsGTT	GRCh38
NC_000023.10:g.19369341_19369343delinsGTT , CM000685.1:g.19369341_19369343delinsGTT	GRCh37
NC_000023.9:g.19279262_19279264delinsGTT	NCBI36
NG_016781.1:g.12331_12333delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.292-37_292-35delinsGTT	ENSP00000348062.6:n.292-37_292-35delinsGTT
ENST00000379805.4:c.292-58_292-56delinsGTT	ENSP00000369133.3:n.292-58_292-56delinsGTT
ENST00000417819.6:c.376-58_376-56delinsGTT	ENSP00000404616.2:n.376-58_376-56delinsGTT
ENST00000423505.6:c.406-58_406-56delinsGTT	ENSP00000406473.2:n.406-58_406-56delinsGTT
ENST00000696704.1:c.292-58_292-56delinsGTT	ENSP00000512823.1:n.292-58_292-56delinsGTT
ENST00000696705.1:c.292-58_292-56delinsGTT	ENSP00000512824.1:n.292-58_292-56delinsGTT
ENST00000422285.7:c.292-58_292-56delinsGTT MANE Select	ENSP00000394382.2:n.292-58_292-56delinsGTT
ENST00000355808.9:c.292-37_292-35delinsGTT	ENSP00000348062.5:n.292-37_292-35delinsGTT
ENST00000379805.3:c.292-58_292-56delinsGTT	ENSP00000369133.3:n.292-58_292-56delinsGTT
ENST00000379806.9:c.406-58_406-56delinsGTT	ENSP00000369134.5:n.406-58_406-56delinsGTT
ENST00000422285.6:c.292-58_292-56delinsGTT	ENSP00000394382.2:n.292-58_292-56delinsGTT
ENST00000423505.5:c.406-58_406-56delinsGTT	ENSP00000406473.1:n.406-58_406-56delinsGTT
ENST00000492364.1:n.394-58_394-56delinsGTT
ENST00000540249.5:c.292-58_292-56delinsGTT	ENSP00000440761.1:n.292-58_292-56delinsGTT
ENST00000545074.5:c.292-37_292-35delinsGTT	ENSP00000438550.1:n.292-37_292-35delinsGTT
NM_000284.3:c.292-58_292-56delinsGTT	NP_000275.1:n.292-58_292-56delinsGTT
NM_001173454.1:c.406-58_406-56delinsGTT	NP_001166925.1:n.406-58_406-56delinsGTT
NM_001173455.1:c.292-37_292-35delinsGTT	NP_001166926.1:n.292-37_292-35delinsGTT
NM_001173456.1:c.292-58_292-56delinsGTT	NP_001166927.1:n.292-58_292-56delinsGTT
XM_011545531.1:c.406-37_406-35delinsGTT	XP_011543833.1:n.406-37_406-35delinsGTT
XM_011545532.1:c.406-37_406-35delinsGTT	XP_011543834.1:n.406-37_406-35delinsGTT
XM_017029574.2:c.406-58_406-56delinsGTT	XP_016885063.1:n.406-58_406-56delinsGTT
NM_000284.4:c.292-58_292-56delinsGTT MANE Select	NP_000275.1:n.292-58_292-56delinsGTT
NM_001173454.2:c.406-58_406-56delinsGTT	NP_001166925.1:n.406-58_406-56delinsGTT
NM_001173455.2:c.292-37_292-35delinsGTT	NP_001166926.1:n.292-37_292-35delinsGTT
NM_001173456.2:c.292-58_292-56delinsGTT	NP_001166927.1:n.292-58_292-56delinsGTT