Canonical Allele Identifier: CA2418225728

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359776T= , CM000685.2:g.19359776T=	GRCh38
NC_000023.10:g.19377894T= , CM000685.1:g.19377894T=	GRCh37
NC_000023.9:g.19287815T=	NCBI36
NG_016781.1:g.20884T=
NG_021184.1:g.160486A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*123T=	ENSP00000348062.6:n.*123T=
ENST00000379805.4:c.*988T=	ENSP00000369133.3:n.*988T=
ENST00000417819.6:c.*123T=	ENSP00000404616.2:n.*123T=
ENST00000423505.6:c.*123T=	ENSP00000406473.2:n.*123T=
ENST00000481733.2:n.1091T=
ENST00000696704.1:c.*628T=	ENSP00000512823.1:n.*628T=
ENST00000696705.1:c.*751T=	ENSP00000512824.1:n.*751T=
ENST00000422285.7:c.*123T= MANE Select	ENSP00000394382.2:n.*123T=
ENST00000379804.1:c.*123T=	ENSP00000369132.1:n.*123T=
ENST00000379806.9:c.*123T=	ENSP00000369134.5:n.*123T=
ENST00000422285.6:c.*123T=	ENSP00000394382.2:n.*123T=
ENST00000478795.1:n.735T=
ENST00000540249.5:c.*123T=	ENSP00000440761.1:n.*123T=
ENST00000545074.5:c.*123T=	ENSP00000438550.1:n.*123T=
NM_000284.3:c.*123T=	NP_000275.1:n.*123T=
NM_001173454.1:c.*123T=	NP_001166925.1:n.*123T=
NM_001173455.1:c.*123T=	NP_001166926.1:n.*123T=
NM_001173456.1:c.*123T=	NP_001166927.1:n.*123T=
XM_011545531.1:c.*123T=	XP_011543833.1:n.*123T=
XM_011545532.1:c.*123T=	XP_011543834.1:n.*123T=
XM_017029574.2:c.*123T=	XP_016885063.1:n.*123T=
NM_000284.4:c.*123T= MANE Select	NP_000275.1:n.*123T=
NM_001173454.2:c.*123T=	NP_001166925.1:n.*123T=
NM_001173455.2:c.*123T=	NP_001166926.1:n.*123T=
NM_001173456.2:c.*123T=	NP_001166927.1:n.*123T=