Canonical Allele Identifier: CA2693251529

Gene: PDHA1

Linked Data

• gnomAD v4: X-19359948-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359948A>G , CM000685.2:g.19359948A>G	GRCh38
NC_000023.10:g.19378066A>G , CM000685.1:g.19378066A>G	GRCh37
NC_000023.9:g.19287987A>G	NCBI36
NG_016781.1:g.21056A>G
NG_021184.1:g.160314T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*295A>G	ENSP00000348062.6:n.*295A>G
ENST00000423505.6:c.*295A>G	ENSP00000406473.2:n.*295A>G
ENST00000696704.1:c.*800A>G	ENSP00000512823.1:n.*800A>G
ENST00000696705.1:c.*923A>G	ENSP00000512824.1:n.*923A>G
ENST00000422285.7:c.*295A>G MANE Select	ENSP00000394382.2:n.*295A>G
ENST00000379806.9:c.*295A>G	ENSP00000369134.5:n.*295A>G
ENST00000422285.6:c.*295A>G	ENSP00000394382.2:n.*295A>G
ENST00000540249.5:c.*295A>G	ENSP00000440761.1:n.*295A>G
ENST00000545074.5:c.*295A>G	ENSP00000438550.1:n.*295A>G
NM_000284.3:c.*295A>G	NP_000275.1:n.*295A>G
NM_001173454.1:c.*295A>G	NP_001166925.1:n.*295A>G
NM_001173455.1:c.*295A>G	NP_001166926.1:n.*295A>G
NM_001173456.1:c.*295A>G	NP_001166927.1:n.*295A>G
XM_011545531.1:c.*295A>G	XP_011543833.1:n.*295A>G
XM_011545532.1:c.*295A>G	XP_011543834.1:n.*295A>G
NM_000284.4:c.*295A>G MANE Select	NP_000275.1:n.*295A>G
NM_001173454.2:c.*295A>G	NP_001166925.1:n.*295A>G
NM_001173455.2:c.*295A>G	NP_001166926.1:n.*295A>G
NM_001173456.2:c.*295A>G	NP_001166927.1:n.*295A>G