Canonical Allele Identifier: CA2418225709

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359752A= , CM000685.2:g.19359752A=	GRCh38
NC_000023.10:g.19377870A= , CM000685.1:g.19377870A=	GRCh37
NC_000023.9:g.19287791A=	NCBI36
NG_016781.1:g.20860A=
NG_021184.1:g.160510T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*99A=	ENSP00000348062.6:n.*99A=
ENST00000379805.4:c.*964A=	ENSP00000369133.3:n.*964A=
ENST00000417819.6:c.*99A=	ENSP00000404616.2:n.*99A=
ENST00000423505.6:c.*99A=	ENSP00000406473.2:n.*99A=
ENST00000481733.2:n.1067A=
ENST00000696704.1:c.*604A=	ENSP00000512823.1:n.*604A=
ENST00000696705.1:c.*727A=	ENSP00000512824.1:n.*727A=
ENST00000422285.7:c.*99A= MANE Select	ENSP00000394382.2:n.*99A=
ENST00000379804.1:c.*99A=	ENSP00000369132.1:n.*99A=
ENST00000379806.9:c.*99A=	ENSP00000369134.5:n.*99A=
ENST00000422285.6:c.*99A=	ENSP00000394382.2:n.*99A=
ENST00000478795.1:n.711A=
ENST00000540249.5:c.*99A=	ENSP00000440761.1:n.*99A=
ENST00000545074.5:c.*99A=	ENSP00000438550.1:n.*99A=
NM_000284.3:c.*99A=	NP_000275.1:n.*99A=
NM_001173454.1:c.*99A=	NP_001166925.1:n.*99A=
NM_001173455.1:c.*99A=	NP_001166926.1:n.*99A=
NM_001173456.1:c.*99A=	NP_001166927.1:n.*99A=
XM_011545531.1:c.*99A=	XP_011543833.1:n.*99A=
XM_011545532.1:c.*99A=	XP_011543834.1:n.*99A=
XM_017029574.2:c.*99A=	XP_016885063.1:n.*99A=
NM_000284.4:c.*99A= MANE Select	NP_000275.1:n.*99A=
NM_001173454.2:c.*99A=	NP_001166925.1:n.*99A=
NM_001173455.2:c.*99A=	NP_001166926.1:n.*99A=
NM_001173456.2:c.*99A=	NP_001166927.1:n.*99A=