Canonical Allele Identifier: CA2693251540
Gene: PDHA1 HGNC NCBI

Linked Data

gnomAD v4: X-19359967-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359967A>T , CM000685.2:g.19359967A>T GRCh38
NC_000023.10:g.19378085A>T , CM000685.1:g.19378085A>T GRCh37
NC_000023.9:g.19288006A>T NCBI36
NG_016781.1:g.21075A>T
NG_021184.1:g.160295T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*314A>T ENSP00000348062.6:n.*314A>T
ENST00000423505.6:c.*314A>T ENSP00000406473.2:n.*314A>T
ENST00000696704.1:c.*819A>T ENSP00000512823.1:n.*819A>T
ENST00000696705.1:c.*942A>T ENSP00000512824.1:n.*942A>T
ENST00000422285.7:c.*314A>T MANE Select ENSP00000394382.2:n.*314A>T
ENST00000379806.9:c.*314A>T ENSP00000369134.5:n.*314A>T
ENST00000422285.6:c.*314A>T ENSP00000394382.2:n.*314A>T
ENST00000540249.5:c.*314A>T ENSP00000440761.1:n.*314A>T
ENST00000545074.5:c.*314A>T ENSP00000438550.1:n.*314A>T
NM_000284.3:c.*314A>T NP_000275.1:n.*314A>T
NM_001173454.1:c.*314A>T NP_001166925.1:n.*314A>T
NM_001173455.1:c.*314A>T NP_001166926.1:n.*314A>T
NM_001173456.1:c.*314A>T NP_001166927.1:n.*314A>T
XM_011545531.1:c.*314A>T XP_011543833.1:n.*314A>T
XM_011545532.1:c.*314A>T XP_011543834.1:n.*314A>T
NM_000284.4:c.*314A>T MANE Select NP_000275.1:n.*314A>T
NM_001173454.2:c.*314A>T NP_001166925.1:n.*314A>T
NM_001173455.2:c.*314A>T NP_001166926.1:n.*314A>T
NM_001173456.2:c.*314A>T NP_001166927.1:n.*314A>T