Canonical Allele Identifier: CA2740044070

Gene: PDHA1

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359656G>T , CM000685.2:g.19359656G>T	GRCh38
NC_000023.10:g.19377774G>T , CM000685.1:g.19377774G>T	GRCh37
NC_000023.9:g.19287695G>T	NCBI36
NG_016781.1:g.20764G>T
NG_021184.1:g.160606C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.*3G>T	ENSP00000348062.6:n.*3G>T
ENST00000379805.4:c.*868G>T	ENSP00000369133.3:n.*868G>T
ENST00000417819.6:c.*3G>T	ENSP00000404616.2:n.*3G>T
ENST00000423505.6:c.*3G>T	ENSP00000406473.2:n.*3G>T
ENST00000481733.2:n.971G>T
ENST00000696704.1:c.*508G>T	ENSP00000512823.1:n.*508G>T
ENST00000696705.1:c.*631G>T	ENSP00000512824.1:n.*631G>T
ENST00000422285.7:c.*3G>T MANE Select	ENSP00000394382.2:n.*3G>T
ENST00000379804.1:c.*3G>T	ENSP00000369132.1:n.*3G>T
ENST00000379806.9:c.*3G>T	ENSP00000369134.5:n.*3G>T
ENST00000422285.6:c.*3G>T	ENSP00000394382.2:n.*3G>T
ENST00000478795.1:n.615G>T
ENST00000540249.5:c.*3G>T	ENSP00000440761.1:n.*3G>T
ENST00000545074.5:c.*3G>T	ENSP00000438550.1:n.*3G>T
NM_000284.3:c.*3G>T	NP_000275.1:n.*3G>T
NM_001173454.1:c.*3G>T	NP_001166925.1:n.*3G>T
NM_001173455.1:c.*3G>T	NP_001166926.1:n.*3G>T
NM_001173456.1:c.*3G>T	NP_001166927.1:n.*3G>T
XM_011545531.1:c.*3G>T	XP_011543833.1:n.*3G>T
XM_011545532.1:c.*3G>T	XP_011543834.1:n.*3G>T
XM_017029574.2:c.*3G>T	XP_016885063.1:n.*3G>T
NM_000284.4:c.*3G>T MANE Select	NP_000275.1:n.*3G>T
NM_001173454.2:c.*3G>T	NP_001166925.1:n.*3G>T
NM_001173455.2:c.*3G>T	NP_001166926.1:n.*3G>T
NM_001173456.2:c.*3G>T	NP_001166927.1:n.*3G>T