Canonical Allele Identifier: CA2693251034

Gene: PDHA1

Linked Data

• gnomAD v4: X-19358828-A-ATCCAACCTCATATCATGTT

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19358835_19358836insTCATATCATGTTTCCAACC , CM000685.2:g.19358835_19358836insTCATATCATGTTTCCAACC	GRCh38
NC_000023.10:g.19376953_19376954insTCATATCATGTTTCCAACC , CM000685.1:g.19376953_19376954insTCATATCATGTTTCCAACC	GRCh37
NC_000023.9:g.19286874_19286875insTCATATCATGTTTCCAACC	NCBI36
NG_016781.1:g.19943_19944insTCATATCATGTTTCCAACC
NG_021184.1:g.161433_161434insAACATGATATGAGGTTGGA

Transcript Alleles

HGVS	Amino-acid change
ENST00000355808.10:c.921-81_921-80insTCATATCATGTTTCCAACC	ENSP00000348062.6:n.921-81_921-80insTCATA...
ENST00000379805.4:c.*592-81_*592-80insTCATATCATGTTTCCAACC	ENSP00000369133.3:n.*592-81_*592-80insTCA...
ENST00000417819.6:c.984-81_984-80insTCATATCATGTTTCCAACC	ENSP00000404616.2:n.984-81_984-80insTCATA...
ENST00000423505.6:c.1014-81_1014-80insTCATATCATGTTTCCAACC	ENSP00000406473.2:n.1014-81_1014-80insTCA...
ENST00000481733.2:n.695-81_695-80insTCATATCATGTTTCCAACC
ENST00000696704.1:c.*232-81_*232-80insTCATATCATGTTTCCAACC	ENSP00000512823.1:n.*232-81_*232-80insTCA...
ENST00000696705.1:c.*355-81_*355-80insTCATATCATGTTTCCAACC	ENSP00000512824.1:n.*355-81_*355-80insTCA...
ENST00000422285.7:c.900-81_900-80insTCATATCATGTTTCCAACC MANE Select	ENSP00000394382.2:n.900-81_900-80insTCATA...
ENST00000379804.1:c.57-81_57-80insTCATATCATGTTTCCAACC	ENSP00000369132.1:n.57-81_57-80insTCATATC...
ENST00000379806.9:c.1014-81_1014-80insTCATATCATGTTTCCAACC	ENSP00000369134.5:n.1014-81_1014-80insTCA...
ENST00000422285.6:c.900-81_900-80insTCATATCATGTTTCCAACC	ENSP00000394382.2:n.900-81_900-80insTCATA...
ENST00000478795.1:n.339-81_339-80insTCATATCATGTTTCCAACC
ENST00000481733.1:n.328-81_328-80insTCATATCATGTTTCCAACC
ENST00000540249.5:c.807-81_807-80insTCATATCATGTTTCCAACC	ENSP00000440761.1:n.807-81_807-80insTCATA...
ENST00000545074.5:c.921-81_921-80insTCATATCATGTTTCCAACC	ENSP00000438550.1:n.921-81_921-80insTCATA...
NM_000284.3:c.900-81_900-80insTCATATCATGTTTCCAACC	NP_000275.1:n.900-81_900-80insTCATATCATGT...
NM_001173454.1:c.1014-81_1014-80insTCATATCATGTTTCCAACC	NP_001166925.1:n.1014-81_1014-80insTCATAT...
NM_001173455.1:c.921-81_921-80insTCATATCATGTTTCCAACC	NP_001166926.1:n.921-81_921-80insTCATATCA...
NM_001173456.1:c.807-81_807-80insTCATATCATGTTTCCAACC	NP_001166927.1:n.807-81_807-80insTCATATCA...
XM_011545531.1:c.1035-81_1035-80insTCATATCATGTTTCCAACC	XP_011543833.1:n.1035-81_1035-80insTCATAT...
XM_011545532.1:c.942-81_942-80insTCATATCATGTTTCCAACC	XP_011543834.1:n.942-81_942-80insTCATATCA...
XM_017029574.2:c.921-81_921-80insTCATATCATGTTTCCAACC	XP_016885063.1:n.921-81_921-80insTCATATCA...
NM_000284.4:c.900-81_900-80insTCATATCATGTTTCCAACC MANE Select	NP_000275.1:n.900-81_900-80insTCATATCATGT...
NM_001173454.2:c.1014-81_1014-80insTCATATCATGTTTCCAACC	NP_001166925.1:n.1014-81_1014-80insTCATAT...
NM_001173455.2:c.921-81_921-80insTCATATCATGTTTCCAACC	NP_001166926.1:n.921-81_921-80insTCATATCA...
NM_001173456.2:c.807-81_807-80insTCATATCATGTTTCCAACC	NP_001166927.1:n.807-81_807-80insTCATATCA...