Canonical Allele Identifier: CA2693251355

Gene: PDHA1

Linked Data

• gnomAD v4: X-19359671-GTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359672_19359673del , CM000685.2:g.19359672_19359673del	GRCh38
NC_000023.10:g.19377790_19377791del , CM000685.1:g.19377790_19377791del	GRCh37
NC_000023.9:g.19287711_19287712del	NCBI36
NG_016781.1:g.20780_20781del
NG_021184.1:g.160589_160590del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*19_*20del	ENSP00000348062.6:n.*19_*20del
ENST00000379805.4:c.*884_*885del	ENSP00000369133.3:n.*884_*885del
ENST00000417819.6:c.*19_*20del	ENSP00000404616.2:n.*19_*20del
ENST00000423505.6:c.*19_*20del	ENSP00000406473.2:n.*19_*20del
ENST00000481733.2:n.987_988del
ENST00000696704.1:c.*524_*525del	ENSP00000512823.1:n.*524_*525del
ENST00000696705.1:c.*647_*648del	ENSP00000512824.1:n.*647_*648del
ENST00000422285.7:c.*19_*20del MANE Select	ENSP00000394382.2:n.*19_*20del
ENST00000379804.1:c.*19_*20del	ENSP00000369132.1:n.*19_*20del
ENST00000379806.9:c.*19_*20del	ENSP00000369134.5:n.*19_*20del
ENST00000422285.6:c.*19_*20del	ENSP00000394382.2:n.*19_*20del
ENST00000478795.1:n.631_632del
ENST00000540249.5:c.*19_*20del	ENSP00000440761.1:n.*19_*20del
ENST00000545074.5:c.*19_*20del	ENSP00000438550.1:n.*19_*20del
NM_000284.3:c.*19_*20del	NP_000275.1:n.*19_*20del
NM_001173454.1:c.*19_*20del	NP_001166925.1:n.*19_*20del
NM_001173455.1:c.*19_*20del	NP_001166926.1:n.*19_*20del
NM_001173456.1:c.*19_*20del	NP_001166927.1:n.*19_*20del
XM_011545531.1:c.*19_*20del	XP_011543833.1:n.*19_*20del
XM_011545532.1:c.*19_*20del	XP_011543834.1:n.*19_*20del
XM_017029574.2:c.*19_*20del	XP_016885063.1:n.*19_*20del
NM_000284.4:c.*19_*20del MANE Select	NP_000275.1:n.*19_*20del
NM_001173454.2:c.*19_*20del	NP_001166925.1:n.*19_*20del
NM_001173455.2:c.*19_*20del	NP_001166926.1:n.*19_*20del
NM_001173456.2:c.*19_*20del	NP_001166927.1:n.*19_*20del