Canonical Allele Identifier: CA2418224984

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358531C= , CM000685.2:g.19358531C=	GRCh38
NC_000023.10:g.19376649C= , CM000685.1:g.19376649C=	GRCh37
NC_000023.9:g.19286570C=	NCBI36
NG_016781.1:g.19639C=
NG_021184.1:g.161731G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.921-385C=	ENSP00000348062.6:n.921-385C=
ENST00000379805.4:c.*592-385C=	ENSP00000369133.3:n.*592-385C=
ENST00000417819.6:c.984-385C=	ENSP00000404616.2:n.984-385C=
ENST00000423505.6:c.1014-385C=	ENSP00000406473.2:n.1014-385C=
ENST00000481733.2:n.695-385C=
ENST00000696704.1:c.*232-385C=	ENSP00000512823.1:n.*232-385C=
ENST00000696705.1:c.*355-385C=	ENSP00000512824.1:n.*355-385C=
ENST00000422285.7:c.900-385C= MANE Select	ENSP00000394382.2:n.900-385C=
ENST00000379804.1:c.57-385C=	ENSP00000369132.1:n.57-385C=
ENST00000379806.9:c.1014-385C=	ENSP00000369134.5:n.1014-385C=
ENST00000422285.6:c.900-385C=	ENSP00000394382.2:n.900-385C=
ENST00000478795.1:n.339-385C=
ENST00000481733.1:n.328-385C=
ENST00000540249.5:c.807-385C=	ENSP00000440761.1:n.807-385C=
ENST00000545074.5:c.921-385C=	ENSP00000438550.1:n.921-385C=
NM_000284.3:c.900-385C=	NP_000275.1:n.900-385C=
NM_001173454.1:c.1014-385C=	NP_001166925.1:n.1014-385C=
NM_001173455.1:c.921-385C=	NP_001166926.1:n.921-385C=
NM_001173456.1:c.807-385C=	NP_001166927.1:n.807-385C=
XM_011545531.1:c.1035-385C=	XP_011543833.1:n.1035-385C=
XM_011545532.1:c.942-385C=	XP_011543834.1:n.942-385C=
XM_017029574.2:c.921-385C=	XP_016885063.1:n.921-385C=
NM_000284.4:c.900-385C= MANE Select	NP_000275.1:n.900-385C=
NM_001173454.2:c.1014-385C=	NP_001166925.1:n.1014-385C=
NM_001173455.2:c.921-385C=	NP_001166926.1:n.921-385C=
NM_001173456.2:c.807-385C=	NP_001166927.1:n.807-385C=