Canonical Allele Identifier: CA2819937208
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359790_19359793dup , CM000685.2:g.19359790_19359793dup GRCh38
NC_000023.10:g.19377908_19377911dup , CM000685.1:g.19377908_19377911dup GRCh37
NC_000023.9:g.19287829_19287832dup NCBI36
NG_016781.1:g.20898_20901dup
NG_021184.1:g.160471_160474dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*137_*140dup ENSP00000348062.6:n.*137_*140dup
ENST00000379805.4:c.*1002_*1005dup ENSP00000369133.3:n.*1002_*1005dup
ENST00000417819.6:c.*137_*140dup ENSP00000404616.2:n.*137_*140dup
ENST00000423505.6:c.*137_*140dup ENSP00000406473.2:n.*137_*140dup
ENST00000481733.2:n.1105_1108dup
ENST00000696704.1:c.*642_*645dup ENSP00000512823.1:n.*642_*645dup
ENST00000696705.1:c.*765_*768dup ENSP00000512824.1:n.*765_*768dup
ENST00000422285.7:c.*137_*140dup MANE Select ENSP00000394382.2:n.*137_*140dup
ENST00000379804.1:c.*137_*140dup ENSP00000369132.1:n.*137_*140dup
ENST00000379806.9:c.*137_*140dup ENSP00000369134.5:n.*137_*140dup
ENST00000422285.6:c.*137_*140dup ENSP00000394382.2:n.*137_*140dup
ENST00000478795.1:n.749_752dup
ENST00000540249.5:c.*137_*140dup ENSP00000440761.1:n.*137_*140dup
ENST00000545074.5:c.*137_*140dup ENSP00000438550.1:n.*137_*140dup
NM_000284.3:c.*137_*140dup NP_000275.1:n.*137_*140dup
NM_001173454.1:c.*137_*140dup NP_001166925.1:n.*137_*140dup
NM_001173455.1:c.*137_*140dup NP_001166926.1:n.*137_*140dup
NM_001173456.1:c.*137_*140dup NP_001166927.1:n.*137_*140dup
XM_011545531.1:c.*137_*140dup XP_011543833.1:n.*137_*140dup
XM_011545532.1:c.*137_*140dup XP_011543834.1:n.*137_*140dup
XM_017029574.2:c.*137_*140dup XP_016885063.1:n.*137_*140dup
NM_000284.4:c.*137_*140dup MANE Select NP_000275.1:n.*137_*140dup
NM_001173454.2:c.*137_*140dup NP_001166925.1:n.*137_*140dup
NM_001173455.2:c.*137_*140dup NP_001166926.1:n.*137_*140dup
NM_001173456.2:c.*137_*140dup NP_001166927.1:n.*137_*140dup