Canonical Allele Identifier: CA2418225979
Gene: PDHA1 HGNC NCBI
MAP3K15 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19360126_19360131delinsTTCCAA , CM000685.2:g.19360126_19360131delinsTTCCAA GRCh38
NC_000023.10:g.19378244_19378249delinsTTCCAA , CM000685.1:g.19378244_19378249delinsTTCCAA GRCh37
NC_000023.9:g.19288165_19288170delinsTTCCAA NCBI36
NG_016781.1:g.21234_21239delinsTTCCAA
NG_021184.1:g.160131_160136delinsTTGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*473_*478delinsTTCCAA (PDHA1) ENSP00000348062.6:n.*473_*478delinsTTCCAA
ENST00000423505.6:c.*473_*478delinsTTCCAA (PDHA1) ENSP00000406473.2:n.*473_*478delinsTTCCAA
ENST00000696704.1:c.*978_*983delinsTTCCAA (PDHA1) ENSP00000512823.1:n.*978_*983delinsTTCCAA
ENST00000696705.1:c.*1101_*1106delinsTTCCAA (PDHA1) ENSP00000512824.1:n.*1101_*1106delinsTTCCAA
ENST00000338883.9:c.*618_*623delinsTTGGAA (MAP3K15) MANE Select ENSP00000345629.4:n.*618_*623delinsTTGGAA
ENST00000422285.7:c.*473_*478delinsTTCCAA (PDHA1) MANE Select ENSP00000394382.2:n.*473_*478delinsTTCCAA
ENST00000359173.7:c.3888_3893delinsTTGGAA (MAP3K15)
ENST00000379806.9:c.*473_*478delinsTTCCAA (PDHA1) ENSP00000369134.5:n.*473_*478delinsTTCCAA
ENST00000422285.6:c.*473_*478delinsTTCCAA (PDHA1) ENSP00000394382.2:n.*473_*478delinsTTCCAA
ENST00000470101.1:n.1978_1983delinsTTGGAA (MAP3K15)
ENST00000518578.5:n.4622_4627delinsTTGGAA (MAP3K15)
ENST00000540249.5:c.*473_*478delinsTTCCAA (PDHA1) ENSP00000440761.1:n.*473_*478delinsTTCCAA
ENST00000545074.5:c.*473_*478delinsTTCCAA (PDHA1) ENSP00000438550.1:n.*473_*478delinsTTCCAA
NM_000284.3:c.*473_*478delinsTTCCAA (PDHA1) NP_000275.1:n.*473_*478delinsTTCCAA
NM_001001671.3:c.4560_4565delinsTTGGAA (MAP3K15) NP_001001671.3:n.4560_4565delinsTTGGAA
NM_001173454.1:c.*473_*478delinsTTCCAA (PDHA1) NP_001166925.1:n.*473_*478delinsTTCCAA
NM_001173455.1:c.*473_*478delinsTTCCAA (PDHA1) NP_001166926.1:n.*473_*478delinsTTCCAA
NM_001173456.1:c.*473_*478delinsTTCCAA (PDHA1) NP_001166927.1:n.*473_*478delinsTTCCAA
XM_011545507.1:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543809.1:n.*618_*623delinsTTGGAA
XM_011545508.1:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543810.1:n.*618_*623delinsTTGGAA
XM_011545509.1:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543811.1:n.*618_*623delinsTTGGAA
XM_011545510.1:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543812.1:n.*618_*623delinsTTGGAA
XM_011545511.1:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543813.1:n.*618_*623delinsTTGGAA
XM_011545531.1:c.*473_*478delinsTTCCAA (PDHA1) XP_011543833.1:n.*473_*478delinsTTCCAA
XM_011545532.1:c.*473_*478delinsTTCCAA (PDHA1) XP_011543834.1:n.*473_*478delinsTTCCAA
XM_011545507.3:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543809.3:n.*618_*623delinsTTGGAA
XM_011545508.3:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543810.3:n.*618_*623delinsTTGGAA
XM_011545510.2:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543812.1:n.*618_*623delinsTTGGAA
XM_011545511.2:c.*618_*623delinsTTGGAA (MAP3K15) XP_011543813.1:n.*618_*623delinsTTGGAA
NM_000284.4:c.*473_*478delinsTTCCAA (PDHA1) MANE Select NP_000275.1:n.*473_*478delinsTTCCAA
NM_001001671.4:c.*618_*623delinsTTGGAA (MAP3K15) MANE Select NP_001001671.3:n.*618_*623delinsTTGGAA
NM_001173454.2:c.*473_*478delinsTTCCAA (PDHA1) NP_001166925.1:n.*473_*478delinsTTCCAA
NM_001173455.2:c.*473_*478delinsTTCCAA (PDHA1) NP_001166926.1:n.*473_*478delinsTTCCAA
NM_001173456.2:c.*473_*478delinsTTCCAA (PDHA1) NP_001166927.1:n.*473_*478delinsTTCCAA