Canonical Allele Identifier: CA2418222081

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19351247T= , CM000685.2:g.19351247T=	GRCh38
NC_000023.10:g.19369365T= , CM000685.1:g.19369365T=	GRCh37
NC_000023.9:g.19279286T=	NCBI36
NG_016781.1:g.12355T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.292-13T=	ENSP00000348062.6:n.292-13T=
ENST00000379805.4:c.292-34T=	ENSP00000369133.3:n.292-34T=
ENST00000417819.6:c.376-34T=	ENSP00000404616.2:n.376-34T=
ENST00000423505.6:c.406-34T=	ENSP00000406473.2:n.406-34T=
ENST00000696704.1:c.292-34T=	ENSP00000512823.1:n.292-34T=
ENST00000696705.1:c.292-34T=	ENSP00000512824.1:n.292-34T=
ENST00000422285.7:c.292-34T= MANE Select	ENSP00000394382.2:n.292-34T=
ENST00000355808.9:c.292-13T=	ENSP00000348062.5:n.292-13T=
ENST00000379805.3:c.292-34T=	ENSP00000369133.3:n.292-34T=
ENST00000379806.9:c.406-34T=	ENSP00000369134.5:n.406-34T=
ENST00000422285.6:c.292-34T=	ENSP00000394382.2:n.292-34T=
ENST00000423505.5:c.406-34T=	ENSP00000406473.1:n.406-34T=
ENST00000492364.1:n.394-34T=
ENST00000540249.5:c.292-34T=	ENSP00000440761.1:n.292-34T=
ENST00000545074.5:c.292-13T=	ENSP00000438550.1:n.292-13T=
NM_000284.3:c.292-34T=	NP_000275.1:n.292-34T=
NM_001173454.1:c.406-34T=	NP_001166925.1:n.406-34T=
NM_001173455.1:c.292-13T=	NP_001166926.1:n.292-13T=
NM_001173456.1:c.292-34T=	NP_001166927.1:n.292-34T=
XM_011545531.1:c.406-13T=	XP_011543833.1:n.406-13T=
XM_011545532.1:c.406-13T=	XP_011543834.1:n.406-13T=
XM_017029574.2:c.406-34T=	XP_016885063.1:n.406-34T=
NM_000284.4:c.292-34T= MANE Select	NP_000275.1:n.292-34T=
NM_001173454.2:c.406-34T=	NP_001166925.1:n.406-34T=
NM_001173455.2:c.292-13T=	NP_001166926.1:n.292-13T=
NM_001173456.2:c.292-34T=	NP_001166927.1:n.292-34T=