Canonical Allele Identifier: CA2418223622

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19355467A= , CM000685.2:g.19355467A=	GRCh38
NC_000023.10:g.19373585A= , CM000685.1:g.19373585A=	GRCh37
NC_000023.9:g.19283506A=	NCBI36
NG_016781.1:g.16575A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.743A=	ENSP00000348062.6:p.Asp248=
ENST00000379805.4:c.*414A=	ENSP00000369133.3:n.*414A=
ENST00000417819.6:c.806A=	ENSP00000404616.2:p.Asp269=
ENST00000423505.6:c.836A=	ENSP00000406473.2:p.Asp279=
ENST00000481733.2:n.517A=
ENST00000696704.1:c.*54A=	ENSP00000512823.1:n.*54A=
ENST00000696705.1:c.*177A=	ENSP00000512824.1:n.*177A=
ENST00000422285.7:c.722A= MANE Select	ENSP00000394382.2:p.Asp241=
ENST00000379806.9:c.836A=	ENSP00000369134.5:p.Asp279=
ENST00000422285.6:c.722A=	ENSP00000394382.2:p.Asp241=
ENST00000481733.1:n.150A=
ENST00000540249.5:c.629A=	ENSP00000440761.1:p.Asp210=
ENST00000545074.5:c.743A=	ENSP00000438550.1:p.Asp248=
NM_000284.3:c.722A=	NP_000275.1:p.Asp241=
NM_001173454.1:c.836A=	NP_001166925.1:p.Asp279=
NM_001173455.1:c.743A=	NP_001166926.1:p.Asp248=
NM_001173456.1:c.629A=	NP_001166927.1:p.Asp210=
XM_011545531.1:c.857A=	XP_011543833.1:p.Asp286=
XM_011545532.1:c.764A=	XP_011543834.1:p.Asp255=
XM_017029574.2:c.743A=	XP_016885063.1:p.Asp248=
NM_000284.4:c.722A= MANE Select	NP_000275.1:p.Asp241=
NM_001173454.2:c.836A=	NP_001166925.1:p.Asp279=
NM_001173455.2:c.743A=	NP_001166926.1:p.Asp248=
NM_001173456.2:c.629A=	NP_001166927.1:p.Asp210=