Canonical Allele Identifier: CA640522232

Gene: PDHA1

Linked Data

• dbSNP Id: rs1368693054
• gnomAD v2: X-19375558-T-TTCTC
• gnomAD v3: X-19357440-T-TTCTC
• gnomAD v4: X-19357440-T-TTCTC
• MyVariant Identifiers: chrX:g.19375558_19375559insTCTC (hg19) ; chrX:g.19357440_19357441insTCTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357440_19357441insTCTC , CM000685.2:g.19357440_19357441insTCTC	GRCh38
NC_000023.10:g.19375558_19375559insTCTC , CM000685.1:g.19375558_19375559insTCTC	GRCh37
NC_000023.9:g.19285479_19285480insTCTC	NCBI36
NG_016781.1:g.18548_18549insTCTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.853-212_853-211insTCTC	ENSP00000348062.6:n.853-212_853-211insTCTC
ENST00000379805.4:c.*524-212_*524-211insTCTC	ENSP00000369133.3:n.*524-212_*524-211insTCTC
ENST00000417819.6:c.916-212_916-211insTCTC	ENSP00000404616.2:n.916-212_916-211insTCTC
ENST00000423505.6:c.946-212_946-211insTCTC	ENSP00000406473.2:n.946-212_946-211insTCTC
ENST00000481733.2:n.627-212_627-211insTCTC
ENST00000696704.1:c.*164-212_*164-211insTCTC	ENSP00000512823.1:n.*164-212_*164-211insTCTC
ENST00000696705.1:c.*287-212_*287-211insTCTC	ENSP00000512824.1:n.*287-212_*287-211insTCTC
ENST00000422285.7:c.832-212_832-211insTCTC MANE Select	ENSP00000394382.2:n.832-212_832-211insTCTC
ENST00000379804.1:c.-12-212_-12-211insTCTC	ENSP00000369132.1:n.-12-212_-12-211insTCTC
ENST00000379806.9:c.946-212_946-211insTCTC	ENSP00000369134.5:n.946-212_946-211insTCTC
ENST00000422285.6:c.832-212_832-211insTCTC	ENSP00000394382.2:n.832-212_832-211insTCTC
ENST00000478795.1:n.59_60insTCTC
ENST00000481733.1:n.260-212_260-211insTCTC
ENST00000540249.5:c.739-212_739-211insTCTC	ENSP00000440761.1:n.739-212_739-211insTCTC
ENST00000545074.5:c.853-212_853-211insTCTC	ENSP00000438550.1:n.853-212_853-211insTCTC
NM_000284.3:c.832-212_832-211insTCTC	NP_000275.1:n.832-212_832-211insTCTC
NM_001173454.1:c.946-212_946-211insTCTC	NP_001166925.1:n.946-212_946-211insTCTC
NM_001173455.1:c.853-212_853-211insTCTC	NP_001166926.1:n.853-212_853-211insTCTC
NM_001173456.1:c.739-212_739-211insTCTC	NP_001166927.1:n.739-212_739-211insTCTC
XM_011545531.1:c.967-212_967-211insTCTC	XP_011543833.1:n.967-212_967-211insTCTC
XM_011545532.1:c.874-212_874-211insTCTC	XP_011543834.1:n.874-212_874-211insTCTC
XM_017029574.2:c.853-212_853-211insTCTC	XP_016885063.1:n.853-212_853-211insTCTC
NM_000284.4:c.832-212_832-211insTCTC MANE Select	NP_000275.1:n.832-212_832-211insTCTC
NM_001173454.2:c.946-212_946-211insTCTC	NP_001166925.1:n.946-212_946-211insTCTC
NM_001173455.2:c.853-212_853-211insTCTC	NP_001166926.1:n.853-212_853-211insTCTC
NM_001173456.2:c.739-212_739-211insTCTC	NP_001166927.1:n.739-212_739-211insTCTC