Canonical Allele Identifier: CA2693251396

Gene: PDHA1

Linked Data

• gnomAD v4: X-19359731-CAGTCAATGAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359733_19359742del , CM000685.2:g.19359733_19359742del	GRCh38
NC_000023.10:g.19377851_19377860del , CM000685.1:g.19377851_19377860del	GRCh37
NC_000023.9:g.19287772_19287781del	NCBI36
NG_016781.1:g.20841_20850del
NG_021184.1:g.160521_160530del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.*80_*89del	ENSP00000348062.6:n.*80_*89del
ENST00000379805.4:c.*945_*954del	ENSP00000369133.3:n.*945_*954del
ENST00000417819.6:c.*80_*89del	ENSP00000404616.2:n.*80_*89del
ENST00000423505.6:c.*80_*89del	ENSP00000406473.2:n.*80_*89del
ENST00000481733.2:n.1048_1057del
ENST00000696704.1:c.*585_*594del	ENSP00000512823.1:n.*585_*594del
ENST00000696705.1:c.*708_*717del	ENSP00000512824.1:n.*708_*717del
ENST00000422285.7:c.*80_*89del MANE Select	ENSP00000394382.2:n.*80_*89del
ENST00000379804.1:c.*80_*89del	ENSP00000369132.1:n.*80_*89del
ENST00000379806.9:c.*80_*89del	ENSP00000369134.5:n.*80_*89del
ENST00000422285.6:c.*80_*89del	ENSP00000394382.2:n.*80_*89del
ENST00000478795.1:n.692_701del
ENST00000540249.5:c.*80_*89del	ENSP00000440761.1:n.*80_*89del
ENST00000545074.5:c.*80_*89del	ENSP00000438550.1:n.*80_*89del
NM_000284.3:c.*80_*89del	NP_000275.1:n.*80_*89del
NM_001173454.1:c.*80_*89del	NP_001166925.1:n.*80_*89del
NM_001173455.1:c.*80_*89del	NP_001166926.1:n.*80_*89del
NM_001173456.1:c.*80_*89del	NP_001166927.1:n.*80_*89del
XM_011545531.1:c.*80_*89del	XP_011543833.1:n.*80_*89del
XM_011545532.1:c.*80_*89del	XP_011543834.1:n.*80_*89del
XM_017029574.2:c.*80_*89del	XP_016885063.1:n.*80_*89del
NM_000284.4:c.*80_*89del MANE Select	NP_000275.1:n.*80_*89del
NM_001173454.2:c.*80_*89del	NP_001166925.1:n.*80_*89del
NM_001173455.2:c.*80_*89del	NP_001166926.1:n.*80_*89del
NM_001173456.2:c.*80_*89del	NP_001166927.1:n.*80_*89del