Canonical Allele Identifier: CA2418221648
Gene: PDHA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19349858A= , CM000685.2:g.19349858A= GRCh38
NC_000023.10:g.19367976A= , CM000685.1:g.19367976A= GRCh37
NC_000023.9:g.19277897A= NCBI36
NG_016781.1:g.10966A=

Transcript Alleles

HGVS Amino-acid change
ENST00000355808.10:c.118-79A= ENSP00000348062.6:n.118-79A=
ENST00000379805.4:c.118-79A= ENSP00000369133.3:n.118-79A=
ENST00000417819.6:c.202-79A= ENSP00000404616.2:n.202-79A=
ENST00000423505.6:c.232-79A= ENSP00000406473.2:n.232-79A=
ENST00000696704.1:c.118-79A= ENSP00000512823.1:n.118-79A=
ENST00000696705.1:c.118-79A= ENSP00000512824.1:n.118-79A=
ENST00000422285.7:c.118-79A= MANE Select ENSP00000394382.2:n.118-79A=
ENST00000355808.9:c.118-79A= ENSP00000348062.5:n.118-79A=
ENST00000379805.3:c.118-79A= ENSP00000369133.3:n.118-79A=
ENST00000379806.9:c.232-79A= ENSP00000369134.5:n.232-79A=
ENST00000417819.5:c.202-79A= ENSP00000404616.1:n.202-79A=
ENST00000422285.6:c.118-79A= ENSP00000394382.2:n.118-79A=
ENST00000423505.5:c.232-79A= ENSP00000406473.1:n.232-79A=
ENST00000492364.1:n.220-79A=
ENST00000540249.5:c.118-79A= ENSP00000440761.1:n.118-79A=
ENST00000545074.5:c.118-79A= ENSP00000438550.1:n.118-79A=
NM_000284.3:c.118-79A= NP_000275.1:n.118-79A=
NM_001173454.1:c.232-79A= NP_001166925.1:n.232-79A=
NM_001173455.1:c.118-79A= NP_001166926.1:n.118-79A=
NM_001173456.1:c.118-79A= NP_001166927.1:n.118-79A=
XM_011545531.1:c.232-79A= XP_011543833.1:n.232-79A=
XM_011545532.1:c.232-79A= XP_011543834.1:n.232-79A=
XM_017029574.2:c.232-79A= XP_016885063.1:n.232-79A=
NM_000284.4:c.118-79A= MANE Select NP_000275.1:n.118-79A=
NM_001173454.2:c.232-79A= NP_001166925.1:n.232-79A=
NM_001173455.2:c.118-79A= NP_001166926.1:n.118-79A=
NM_001173456.2:c.118-79A= NP_001166927.1:n.118-79A=