Canonical Allele Identifier: CA2418225922

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19360043G= , CM000685.2:g.19360043G=	GRCh38
NC_000023.10:g.19378161G= , CM000685.1:g.19378161G=	GRCh37
NC_000023.9:g.19288082G=	NCBI36
NG_016781.1:g.21151G=
NG_021184.1:g.160219C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*390G=	ENSP00000348062.6:n.*390G=
ENST00000423505.6:c.*390G=	ENSP00000406473.2:n.*390G=
ENST00000696704.1:c.*895G=	ENSP00000512823.1:n.*895G=
ENST00000696705.1:c.*1018G=	ENSP00000512824.1:n.*1018G=
ENST00000422285.7:c.*390G= MANE Select	ENSP00000394382.2:n.*390G=
ENST00000379806.9:c.*390G=	ENSP00000369134.5:n.*390G=
ENST00000422285.6:c.*390G=	ENSP00000394382.2:n.*390G=
ENST00000540249.5:c.*390G=	ENSP00000440761.1:n.*390G=
ENST00000545074.5:c.*390G=	ENSP00000438550.1:n.*390G=
NM_000284.3:c.*390G=	NP_000275.1:n.*390G=
NM_001173454.1:c.*390G=	NP_001166925.1:n.*390G=
NM_001173455.1:c.*390G=	NP_001166926.1:n.*390G=
NM_001173456.1:c.*390G=	NP_001166927.1:n.*390G=
XM_011545531.1:c.*390G=	XP_011543833.1:n.*390G=
XM_011545532.1:c.*390G=	XP_011543834.1:n.*390G=
NM_000284.4:c.*390G= MANE Select	NP_000275.1:n.*390G=
NM_001173454.2:c.*390G=	NP_001166925.1:n.*390G=
NM_001173455.2:c.*390G=	NP_001166926.1:n.*390G=
NM_001173456.2:c.*390G=	NP_001166927.1:n.*390G=