Canonical Allele Identifier: CA2418225867
Gene: PDHA1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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