Canonical Allele Identifier: CA640521573

Gene: PDHA1

Linked Data

• gnomAD v2: X-19371370-A-ATGT
• MyVariant Identifiers: chrX:g.19371370_19371371insTGT (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19353252_19353253insTGT , CM000685.2:g.19353252_19353253insTGT	GRCh38
NC_000023.10:g.19371370_19371371insTGT , CM000685.1:g.19371370_19371371insTGT	GRCh37
NC_000023.9:g.19281291_19281292insTGT	NCBI36
NG_016781.1:g.14360_14361insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.531+79_531+80insTGT	ENSP00000348062.6:n.531+79_531+80insTGT
ENST00000379805.4:c.*46_*47insTGT	ENSP00000369133.3:n.*46_*47insTGT
ENST00000417819.6:c.594+79_594+80insTGT	ENSP00000404616.2:n.594+79_594+80insTGT
ENST00000423505.6:c.624+79_624+80insTGT	ENSP00000406473.2:n.624+79_624+80insTGT
ENST00000696704.1:c.418+1845_418+1846insTGT	ENSP00000512823.1:n.418+1845_418+1846insTGT
ENST00000696705.1:c.419-1239_419-1238insTGT	ENSP00000512824.1:n.419-1239_419-1238insTGT
ENST00000422285.7:c.510+79_510+80insTGT MANE Select	ENSP00000394382.2:n.510+79_510+80insTGT
ENST00000355808.9:c.531+79_531+80insTGT	ENSP00000348062.5:n.531+79_531+80insTGT
ENST00000379805.3:c.*46_*47insTGT	ENSP00000369133.3:n.*46_*47insTGT
ENST00000379806.9:c.624+79_624+80insTGT	ENSP00000369134.5:n.624+79_624+80insTGT
ENST00000422285.6:c.510+79_510+80insTGT	ENSP00000394382.2:n.510+79_510+80insTGT
ENST00000479146.1:n.345+79_345+80insTGT
ENST00000540249.5:c.510+79_510+80insTGT	ENSP00000440761.1:n.510+79_510+80insTGT
ENST00000545074.5:c.531+79_531+80insTGT	ENSP00000438550.1:n.531+79_531+80insTGT
NM_000284.3:c.510+79_510+80insTGT	NP_000275.1:n.510+79_510+80insTGT
NM_001173454.1:c.624+79_624+80insTGT	NP_001166925.1:n.624+79_624+80insTGT
NM_001173455.1:c.531+79_531+80insTGT	NP_001166926.1:n.531+79_531+80insTGT
NM_001173456.1:c.510+79_510+80insTGT	NP_001166927.1:n.510+79_510+80insTGT
XM_011545531.1:c.645+79_645+80insTGT	XP_011543833.1:n.645+79_645+80insTGT
XM_011545532.1:c.645+79_645+80insTGT	XP_011543834.1:n.645+79_645+80insTGT
XM_017029574.2:c.624+79_624+80insTGT	XP_016885063.1:n.624+79_624+80insTGT
NM_000284.4:c.510+79_510+80insTGT MANE Select	NP_000275.1:n.510+79_510+80insTGT
NM_001173454.2:c.624+79_624+80insTGT	NP_001166925.1:n.624+79_624+80insTGT
NM_001173455.2:c.531+79_531+80insTGT	NP_001166926.1:n.531+79_531+80insTGT
NM_001173456.2:c.510+79_510+80insTGT	NP_001166927.1:n.510+79_510+80insTGT