Canonical Allele Identifier: CA2418225976
Gene: PDHA1 HGNC NCBI
MAP3K15 HGNC NCBI

Linked Data

dbSNP Id: rs2063262599

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.19360124_19360126dup , CM000685.2:g.19360124_19360126dup GRCh38
NC_000023.10:g.19378242_19378244dup , CM000685.1:g.19378242_19378244dup GRCh37
NC_000023.9:g.19288163_19288165dup NCBI36
NG_016781.1:g.21232_21234dup
NG_021184.1:g.160138_160140dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000355808.10:c.*471_*473dup (PDHA1) ENSP00000348062.6:n.*471_*473dup
ENST00000423505.6:c.*471_*473dup (PDHA1) ENSP00000406473.2:n.*471_*473dup
ENST00000696704.1:c.*976_*978dup (PDHA1) ENSP00000512823.1:n.*976_*978dup
ENST00000696705.1:c.*1099_*1101dup (PDHA1) ENSP00000512824.1:n.*1099_*1101dup
ENST00000338883.9:c.*625_*627dup (MAP3K15) MANE Select ENSP00000345629.4:n.*625_*627dup
ENST00000422285.7:c.*471_*473dup (PDHA1) MANE Select ENSP00000394382.2:n.*471_*473dup
ENST00000359173.7:c.3895_3897dup (MAP3K15)
ENST00000379806.9:c.*471_*473dup (PDHA1) ENSP00000369134.5:n.*471_*473dup
ENST00000422285.6:c.*471_*473dup (PDHA1) ENSP00000394382.2:n.*471_*473dup
ENST00000470101.1:n.1985_1987dup (MAP3K15)
ENST00000518578.5:n.4629_4631dup (MAP3K15)
ENST00000540249.5:c.*471_*473dup (PDHA1) ENSP00000440761.1:n.*471_*473dup
ENST00000545074.5:c.*471_*473dup (PDHA1) ENSP00000438550.1:n.*471_*473dup
NM_000284.3:c.*471_*473dup (PDHA1) NP_000275.1:n.*471_*473dup
NM_001001671.3:c.4567_4569dup (MAP3K15) NP_001001671.3:n.4567_4569dup
NM_001173454.1:c.*471_*473dup (PDHA1) NP_001166925.1:n.*471_*473dup
NM_001173455.1:c.*471_*473dup (PDHA1) NP_001166926.1:n.*471_*473dup
NM_001173456.1:c.*471_*473dup (PDHA1) NP_001166927.1:n.*471_*473dup
XM_011545507.1:c.*625_*627dup (MAP3K15) XP_011543809.1:n.*625_*627dup
XM_011545508.1:c.*625_*627dup (MAP3K15) XP_011543810.1:n.*625_*627dup
XM_011545509.1:c.*625_*627dup (MAP3K15) XP_011543811.1:n.*625_*627dup
XM_011545510.1:c.*625_*627dup (MAP3K15) XP_011543812.1:n.*625_*627dup
XM_011545511.1:c.*625_*627dup (MAP3K15) XP_011543813.1:n.*625_*627dup
XM_011545531.1:c.*471_*473dup (PDHA1) XP_011543833.1:n.*471_*473dup
XM_011545532.1:c.*471_*473dup (PDHA1) XP_011543834.1:n.*471_*473dup
XM_011545507.3:c.*625_*627dup (MAP3K15) XP_011543809.3:n.*625_*627dup
XM_011545508.3:c.*625_*627dup (MAP3K15) XP_011543810.3:n.*625_*627dup
XM_011545510.2:c.*625_*627dup (MAP3K15) XP_011543812.1:n.*625_*627dup
XM_011545511.2:c.*625_*627dup (MAP3K15) XP_011543813.1:n.*625_*627dup
NM_000284.4:c.*471_*473dup (PDHA1) MANE Select NP_000275.1:n.*471_*473dup
NM_001001671.4:c.*625_*627dup (MAP3K15) MANE Select NP_001001671.3:n.*625_*627dup
NM_001173454.2:c.*471_*473dup (PDHA1) NP_001166925.1:n.*471_*473dup
NM_001173455.2:c.*471_*473dup (PDHA1) NP_001166926.1:n.*471_*473dup
NM_001173456.2:c.*471_*473dup (PDHA1) NP_001166927.1:n.*471_*473dup