Canonical Allele Identifier: CA412396976
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359592G>T , CM000685.2:g.19359592G>T GRCh38
NC_000023.10:g.19377710G>T , CM000685.1:g.19377710G>T GRCh37
NC_000023.9:g.19287631G>T NCBI36
NG_016781.1:g.20700G>T
NG_021184.1:g.160670C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.1133G>T ENSP00000348062.6:p.Ser378Ile
ENST00000379805.4:c.*804G>T ENSP00000369133.3:n.*804G>T
ENST00000417819.6:c.1196G>T ENSP00000404616.2:p.Ser399Ile
ENST00000423505.6:c.1226G>T ENSP00000406473.2:p.Ser409Ile
ENST00000481733.2:n.907G>T
ENST00000696704.1:c.*444G>T ENSP00000512823.1:n.*444G>T
ENST00000696705.1:c.*567G>T ENSP00000512824.1:n.*567G>T
ENST00000422285.7:c.1112G>T MANE Select ENSP00000394382.2:p.Ser371Ile
ENST00000379804.1:c.269G>T ENSP00000369132.1:p.Ser90Ile
ENST00000379806.9:c.1226G>T ENSP00000369134.5:p.Ser409Ile
ENST00000422285.6:c.1112G>T ENSP00000394382.2:p.Ser371Ile
ENST00000478795.1:n.551G>T
ENST00000540249.5:c.1019G>T ENSP00000440761.1:p.Ser340Ile
ENST00000545074.5:c.1133G>T ENSP00000438550.1:p.Ser378Ile
NM_000284.3:c.1112G>T NP_000275.1:p.Ser371Ile
NM_001173454.1:c.1226G>T NP_001166925.1:p.Ser409Ile
NM_001173455.1:c.1133G>T NP_001166926.1:p.Ser378Ile
NM_001173456.1:c.1019G>T NP_001166927.1:p.Ser340Ile
XM_011545531.1:c.1247G>T XP_011543833.1:p.Ser416Ile
XM_011545532.1:c.1154G>T XP_011543834.1:p.Ser385Ile
XM_017029574.2:c.1133G>T XP_016885063.1:p.Ser378Ile
NM_000284.4:c.1112G>T MANE Select NP_000275.1:p.Ser371Ile
NM_001173454.2:c.1226G>T NP_001166925.1:p.Ser409Ile
NM_001173455.2:c.1133G>T NP_001166926.1:p.Ser378Ile
NM_001173456.2:c.1019G>T NP_001166927.1:p.Ser340Ile