Canonical Allele Identifier: CA2418221591

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19349630C= , CM000685.2:g.19349630C=	GRCh38
NC_000023.10:g.19367748C= , CM000685.1:g.19367748C=	GRCh37
NC_000023.9:g.19277669C=	NCBI36
NG_016781.1:g.10738C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.117+259C=	ENSP00000348062.6:n.117+259C=
ENST00000379805.4:c.117+259C=	ENSP00000369133.3:n.117+259C=
ENST00000417819.6:c.201+259C=	ENSP00000404616.2:n.201+259C=
ENST00000423505.6:c.231+259C=	ENSP00000406473.2:n.231+259C=
ENST00000696704.1:c.117+259C=	ENSP00000512823.1:n.117+259C=
ENST00000696705.1:c.117+259C=	ENSP00000512824.1:n.117+259C=
ENST00000422285.7:c.117+259C= MANE Select	ENSP00000394382.2:n.117+259C=
ENST00000355808.9:c.117+259C=	ENSP00000348062.5:n.117+259C=
ENST00000379805.3:c.117+259C=	ENSP00000369133.3:n.117+259C=
ENST00000379806.9:c.231+259C=	ENSP00000369134.5:n.231+259C=
ENST00000417819.5:c.201+259C=	ENSP00000404616.1:n.201+259C=
ENST00000422285.6:c.117+259C=	ENSP00000394382.2:n.117+259C=
ENST00000423505.5:c.231+259C=	ENSP00000406473.1:n.231+259C=
ENST00000492364.1:n.219+259C=
ENST00000540249.5:c.117+259C=	ENSP00000440761.1:n.117+259C=
ENST00000545074.5:c.117+259C=	ENSP00000438550.1:n.117+259C=
NM_000284.3:c.117+259C=	NP_000275.1:n.117+259C=
NM_001173454.1:c.231+259C=	NP_001166925.1:n.231+259C=
NM_001173455.1:c.117+259C=	NP_001166926.1:n.117+259C=
NM_001173456.1:c.117+259C=	NP_001166927.1:n.117+259C=
XM_011545531.1:c.231+259C=	XP_011543833.1:n.231+259C=
XM_011545532.1:c.231+259C=	XP_011543834.1:n.231+259C=
XM_017029574.2:c.231+259C=	XP_016885063.1:n.231+259C=
NM_000284.4:c.117+259C= MANE Select	NP_000275.1:n.117+259C=
NM_001173454.2:c.231+259C=	NP_001166925.1:n.231+259C=
NM_001173455.2:c.117+259C=	NP_001166926.1:n.117+259C=
NM_001173456.2:c.117+259C=	NP_001166927.1:n.117+259C=