Canonical Allele Identifier: CA873741508

Gene: PDHA1

Linked Data

• dbSNP Id: rs1327175282
• gnomAD v3: X-19358594-T-TA
• gnomAD v4: X-19358594-T-TA
• MyVariant Identifiers: chrX:g.19376712_19376713insA (hg19) ; chrX:g.19358594_19358595insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358597dup , CM000685.2:g.19358597dup	GRCh38
NC_000023.10:g.19376715dup , CM000685.1:g.19376715dup	GRCh37
NC_000023.9:g.19286636dup	NCBI36
NG_016781.1:g.19705dup
NG_021184.1:g.161667dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.921-319dup	ENSP00000348062.6:n.921-319dup
ENST00000379805.4:c.*592-319dup	ENSP00000369133.3:n.*592-319dup
ENST00000417819.6:c.984-319dup	ENSP00000404616.2:n.984-319dup
ENST00000423505.6:c.1014-319dup	ENSP00000406473.2:n.1014-319dup
ENST00000481733.2:n.695-319dup
ENST00000696704.1:c.*232-319dup	ENSP00000512823.1:n.*232-319dup
ENST00000696705.1:c.*355-319dup	ENSP00000512824.1:n.*355-319dup
ENST00000422285.7:c.900-319dup MANE Select	ENSP00000394382.2:n.900-319dup
ENST00000379804.1:c.57-319dup	ENSP00000369132.1:n.57-319dup
ENST00000379806.9:c.1014-319dup	ENSP00000369134.5:n.1014-319dup
ENST00000422285.6:c.900-319dup	ENSP00000394382.2:n.900-319dup
ENST00000478795.1:n.339-319dup
ENST00000481733.1:n.328-319dup
ENST00000540249.5:c.807-319dup	ENSP00000440761.1:n.807-319dup
ENST00000545074.5:c.921-319dup	ENSP00000438550.1:n.921-319dup
NM_000284.3:c.900-319dup	NP_000275.1:n.900-319dup
NM_001173454.1:c.1014-319dup	NP_001166925.1:n.1014-319dup
NM_001173455.1:c.921-319dup	NP_001166926.1:n.921-319dup
NM_001173456.1:c.807-319dup	NP_001166927.1:n.807-319dup
XM_011545531.1:c.1035-319dup	XP_011543833.1:n.1035-319dup
XM_011545532.1:c.942-319dup	XP_011543834.1:n.942-319dup
XM_017029574.2:c.921-319dup	XP_016885063.1:n.921-319dup
NM_000284.4:c.900-319dup MANE Select	NP_000275.1:n.900-319dup
NM_001173454.2:c.1014-319dup	NP_001166925.1:n.1014-319dup
NM_001173455.2:c.921-319dup	NP_001166926.1:n.921-319dup
NM_001173456.2:c.807-319dup	NP_001166927.1:n.807-319dup