Canonical Allele Identifier: CA873740885

Gene: PDHA1

Linked Data

• dbSNP Id: rs1210148467
• gnomAD v3: X-19357862-T-TGAAAGCAGTGCCTCCTAATAA
• gnomAD v4: X-19357862-T-TGAAAGCAGTGCCTCCTAATAA
• MyVariant Identifiers: chrX:g.19375980_19375981insGAAAGCAGTGCCTCCTAATAA (hg19) ; chrX:g.19357862_19357863insGAAAGCAGTGCCTCCTAATAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19357869_19357889dup , CM000685.2:g.19357869_19357889dup	GRCh38
NC_000023.10:g.19375987_19376007dup , CM000685.1:g.19375987_19376007dup	GRCh37
NC_000023.9:g.19285908_19285928dup	NCBI36
NG_016781.1:g.18977_18997dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.920+150_920+170dup	ENSP00000348062.6:n.920+150_920+170dup
ENST00000379805.4:c.*591+150_*591+170dup	ENSP00000369133.3:n.*591+150_*591+170dup
ENST00000417819.6:c.983+150_983+170dup	ENSP00000404616.2:n.983+150_983+170dup
ENST00000423505.6:c.1013+150_1013+170dup	ENSP00000406473.2:n.1013+150_1013+170dup
ENST00000481733.2:n.694+150_694+170dup
ENST00000696704.1:c.*231+150_*231+170dup	ENSP00000512823.1:n.*231+150_*231+170dup
ENST00000696705.1:c.*354+150_*354+170dup	ENSP00000512824.1:n.*354+150_*354+170dup
ENST00000422285.7:c.899+150_899+170dup MANE Select	ENSP00000394382.2:n.899+150_899+170dup
ENST00000379804.1:c.56+150_56+170dup	ENSP00000369132.1:n.56+150_56+170dup
ENST00000379806.9:c.1013+150_1013+170dup	ENSP00000369134.5:n.1013+150_1013+170dup
ENST00000422285.6:c.899+150_899+170dup	ENSP00000394382.2:n.899+150_899+170dup
ENST00000478795.1:n.338+150_338+170dup
ENST00000481733.1:n.327+150_327+170dup
ENST00000540249.5:c.806+150_806+170dup	ENSP00000440761.1:n.806+150_806+170dup
ENST00000545074.5:c.920+150_920+170dup	ENSP00000438550.1:n.920+150_920+170dup
NM_000284.3:c.899+150_899+170dup	NP_000275.1:n.899+150_899+170dup
NM_001173454.1:c.1013+150_1013+170dup	NP_001166925.1:n.1013+150_1013+170dup
NM_001173455.1:c.920+150_920+170dup	NP_001166926.1:n.920+150_920+170dup
NM_001173456.1:c.806+150_806+170dup	NP_001166927.1:n.806+150_806+170dup
XM_011545531.1:c.1034+150_1034+170dup	XP_011543833.1:n.1034+150_1034+170dup
XM_011545532.1:c.941+150_941+170dup	XP_011543834.1:n.941+150_941+170dup
XM_017029574.2:c.920+150_920+170dup	XP_016885063.1:n.920+150_920+170dup
NM_000284.4:c.899+150_899+170dup MANE Select	NP_000275.1:n.899+150_899+170dup
NM_001173454.2:c.1013+150_1013+170dup	NP_001166925.1:n.1013+150_1013+170dup
NM_001173455.2:c.920+150_920+170dup	NP_001166926.1:n.920+150_920+170dup
NM_001173456.2:c.806+150_806+170dup	NP_001166927.1:n.806+150_806+170dup