Canonical Allele Identifier: CA2693251356
Gene: PDHA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19359673_19359682dup , CM000685.2:g.19359673_19359682dup GRCh38
NC_000023.10:g.19377791_19377800dup , CM000685.1:g.19377791_19377800dup GRCh37
NC_000023.9:g.19287712_19287721dup NCBI36
NG_016781.1:g.20781_20790dup
NG_021184.1:g.160580_160589dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*20_*29dup ENSP00000348062.6:n.*20_*29dup
ENST00000379805.4:c.*885_*894dup ENSP00000369133.3:n.*885_*894dup
ENST00000417819.6:c.*20_*29dup ENSP00000404616.2:n.*20_*29dup
ENST00000423505.6:c.*20_*29dup ENSP00000406473.2:n.*20_*29dup
ENST00000481733.2:n.988_997dup
ENST00000696704.1:c.*525_*534dup ENSP00000512823.1:n.*525_*534dup
ENST00000696705.1:c.*648_*657dup ENSP00000512824.1:n.*648_*657dup
ENST00000422285.7:c.*20_*29dup MANE Select ENSP00000394382.2:n.*20_*29dup
ENST00000379804.1:c.*20_*29dup ENSP00000369132.1:n.*20_*29dup
ENST00000379806.9:c.*20_*29dup ENSP00000369134.5:n.*20_*29dup
ENST00000422285.6:c.*20_*29dup ENSP00000394382.2:n.*20_*29dup
ENST00000478795.1:n.632_641dup
ENST00000540249.5:c.*20_*29dup ENSP00000440761.1:n.*20_*29dup
ENST00000545074.5:c.*20_*29dup ENSP00000438550.1:n.*20_*29dup
NM_000284.3:c.*20_*29dup NP_000275.1:n.*20_*29dup
NM_001173454.1:c.*20_*29dup NP_001166925.1:n.*20_*29dup
NM_001173455.1:c.*20_*29dup NP_001166926.1:n.*20_*29dup
NM_001173456.1:c.*20_*29dup NP_001166927.1:n.*20_*29dup
XM_011545531.1:c.*20_*29dup XP_011543833.1:n.*20_*29dup
XM_011545532.1:c.*20_*29dup XP_011543834.1:n.*20_*29dup
XM_017029574.2:c.*20_*29dup XP_016885063.1:n.*20_*29dup
NM_000284.4:c.*20_*29dup MANE Select NP_000275.1:n.*20_*29dup
NM_001173454.2:c.*20_*29dup NP_001166925.1:n.*20_*29dup
NM_001173455.2:c.*20_*29dup NP_001166926.1:n.*20_*29dup
NM_001173456.2:c.*20_*29dup NP_001166927.1:n.*20_*29dup