Canonical Allele Identifier: CA2693251182

Gene: PDHA1

Linked Data

• gnomAD v4: X-19359140-A-AATAGGTCCATAGTTCC

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.19359144_19359145insGTCCATAGTTCCATAG , CM000685.2:g.19359144_19359145insGTCCATAGTTCCATAG	GRCh38
NC_000023.10:g.19377262_19377263insGTCCATAGTTCCATAG , CM000685.1:g.19377262_19377263insGTCCATAGTTCCATAG	GRCh37
NC_000023.9:g.19287183_19287184insGTCCATAGTTCCATAG	NCBI36
NG_016781.1:g.20252_20253insGTCCATAGTTCCATAG
NG_021184.1:g.161121_161122insGGAACTATGGACCTAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355808.10:c.1029+120_1029+121insGTCCATAGTTCCATAG	ENSP00000348062.6:n.1029+120_1029+121insGTCCATAGTTCCATAG
ENST00000379805.4:c.*700+120_*700+121insGTCCATAGTTCCATAG	ENSP00000369133.3:n.*700+120_*700+121insGTCCATAGTTCCATAG
ENST00000417819.6:c.1092+120_1092+121insGTCCATAGTTCCATAG	ENSP00000404616.2:n.1092+120_1092+121insGTCCATAGTTCCATAG
ENST00000423505.6:c.1122+120_1122+121insGTCCATAGTTCCATAG	ENSP00000406473.2:n.1122+120_1122+121insGTCCATAGTTCCATAG
ENST00000481733.2:n.803+120_803+121insGTCCATAGTTCCATAG
ENST00000696704.1:c.*340+120_*340+121insGTCCATAGTTCCATAG	ENSP00000512823.1:n.*340+120_*340+121insGTCCATAGTTCCATAG
ENST00000696705.1:c.*463+120_*463+121insGTCCATAGTTCCATAG	ENSP00000512824.1:n.*463+120_*463+121insGTCCATAGTTCCATAG
ENST00000422285.7:c.1008+120_1008+121insGTCCATAGTTCCATAG MANE Select	ENSP00000394382.2:n.1008+120_1008+121insGTCCATAGTTCCATAG
ENST00000379804.1:c.165+120_165+121insGTCCATAGTTCCATAG	ENSP00000369132.1:n.165+120_165+121insGTCCATAGTTCCATAG
ENST00000379806.9:c.1122+120_1122+121insGTCCATAGTTCCATAG	ENSP00000369134.5:n.1122+120_1122+121insGTCCATAGTTCCATAG
ENST00000422285.6:c.1008+120_1008+121insGTCCATAGTTCCATAG	ENSP00000394382.2:n.1008+120_1008+121insGTCCATAGTTCCATAG
ENST00000478795.1:n.447+120_447+121insGTCCATAGTTCCATAG
ENST00000540249.5:c.915+120_915+121insGTCCATAGTTCCATAG	ENSP00000440761.1:n.915+120_915+121insGTCCATAGTTCCATAG
ENST00000545074.5:c.1029+120_1029+121insGTCCATAGTTCCATAG	ENSP00000438550.1:n.1029+120_1029+121insGTCCATAGTTCCATAG
NM_000284.3:c.1008+120_1008+121insGTCCATAGTTCCATAG	NP_000275.1:n.1008+120_1008+121insGTCCATAGTTCCATAG
NM_001173454.1:c.1122+120_1122+121insGTCCATAGTTCCATAG	NP_001166925.1:n.1122+120_1122+121insGTCCATAGTTCCATAG
NM_001173455.1:c.1029+120_1029+121insGTCCATAGTTCCATAG	NP_001166926.1:n.1029+120_1029+121insGTCCATAGTTCCATAG
NM_001173456.1:c.915+120_915+121insGTCCATAGTTCCATAG	NP_001166927.1:n.915+120_915+121insGTCCATAGTTCCATAG
XM_011545531.1:c.1143+120_1143+121insGTCCATAGTTCCATAG	XP_011543833.1:n.1143+120_1143+121insGTCCATAGTTCCATAG
XM_011545532.1:c.1050+120_1050+121insGTCCATAGTTCCATAG	XP_011543834.1:n.1050+120_1050+121insGTCCATAGTTCCATAG
XM_017029574.2:c.1029+120_1029+121insGTCCATAGTTCCATAG	XP_016885063.1:n.1029+120_1029+121insGTCCATAGTTCCATAG
NM_000284.4:c.1008+120_1008+121insGTCCATAGTTCCATAG MANE Select	NP_000275.1:n.1008+120_1008+121insGTCCATAGTTCCATAG
NM_001173454.2:c.1122+120_1122+121insGTCCATAGTTCCATAG	NP_001166925.1:n.1122+120_1122+121insGTCCATAGTTCCATAG
NM_001173455.2:c.1029+120_1029+121insGTCCATAGTTCCATAG	NP_001166926.1:n.1029+120_1029+121insGTCCATAGTTCCATAG
NM_001173456.2:c.915+120_915+121insGTCCATAGTTCCATAG	NP_001166927.1:n.915+120_915+121insGTCCATAGTTCCATAG