Canonical Allele Identifier: CA873741449

Gene: PDHA1

Linked Data

• dbSNP Id: rs1258303346
• gnomAD v3: X-19358479-C-CTGATGTCTCAAAGTCTAA
• gnomAD v4: X-19358479-C-CTGATGTCTCAAAGTCTAA
• MyVariant Identifiers: chrX:g.19376597_19376598insTGATGTCTCAAAGTCTAA (hg19) ; chrX:g.19358479_19358480insTGATGTCTCAAAGTCTAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358481_19358498dup , CM000685.2:g.19358481_19358498dup	GRCh38
NC_000023.10:g.19376599_19376616dup , CM000685.1:g.19376599_19376616dup	GRCh37
NC_000023.9:g.19286520_19286537dup	NCBI36
NG_016781.1:g.19589_19606dup
NG_021184.1:g.161765_161782dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.921-435_921-418dup	ENSP00000348062.6:n.921-435_921-418dup
ENST00000379805.4:c.*592-435_*592-418dup	ENSP00000369133.3:n.*592-435_*592-418dup
ENST00000417819.6:c.984-435_984-418dup	ENSP00000404616.2:n.984-435_984-418dup
ENST00000423505.6:c.1014-435_1014-418dup	ENSP00000406473.2:n.1014-435_1014-418dup
ENST00000481733.2:n.695-435_695-418dup
ENST00000696704.1:c.*232-435_*232-418dup	ENSP00000512823.1:n.*232-435_*232-418dup
ENST00000696705.1:c.*355-435_*355-418dup	ENSP00000512824.1:n.*355-435_*355-418dup
ENST00000422285.7:c.900-435_900-418dup MANE Select	ENSP00000394382.2:n.900-435_900-418dup
ENST00000379804.1:c.57-435_57-418dup	ENSP00000369132.1:n.57-435_57-418dup
ENST00000379806.9:c.1014-435_1014-418dup	ENSP00000369134.5:n.1014-435_1014-418dup
ENST00000422285.6:c.900-435_900-418dup	ENSP00000394382.2:n.900-435_900-418dup
ENST00000478795.1:n.339-435_339-418dup
ENST00000481733.1:n.328-435_328-418dup
ENST00000540249.5:c.807-435_807-418dup	ENSP00000440761.1:n.807-435_807-418dup
ENST00000545074.5:c.921-435_921-418dup	ENSP00000438550.1:n.921-435_921-418dup
NM_000284.3:c.900-435_900-418dup	NP_000275.1:n.900-435_900-418dup
NM_001173454.1:c.1014-435_1014-418dup	NP_001166925.1:n.1014-435_1014-418dup
NM_001173455.1:c.921-435_921-418dup	NP_001166926.1:n.921-435_921-418dup
NM_001173456.1:c.807-435_807-418dup	NP_001166927.1:n.807-435_807-418dup
XM_011545531.1:c.1035-435_1035-418dup	XP_011543833.1:n.1035-435_1035-418dup
XM_011545532.1:c.942-435_942-418dup	XP_011543834.1:n.942-435_942-418dup
XM_017029574.2:c.921-435_921-418dup	XP_016885063.1:n.921-435_921-418dup
NM_000284.4:c.900-435_900-418dup MANE Select	NP_000275.1:n.900-435_900-418dup
NM_001173454.2:c.1014-435_1014-418dup	NP_001166925.1:n.1014-435_1014-418dup
NM_001173455.2:c.921-435_921-418dup	NP_001166926.1:n.921-435_921-418dup
NM_001173456.2:c.807-435_807-418dup	NP_001166927.1:n.807-435_807-418dup