Linked Data
ClinVar Variation Id:
2937548
ClinVar RCV Id:
RCV003794178
dbSNP Id:
rs1169953238
gnomAD v2:
2-26414233-G-A
gnomAD v4:
2-26191364-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26191364G>A , CM000664.2:g.26191364G>A | GRCh38 |
| NC_000002.11:g.26414233G>A , CM000664.1:g.26414233G>A | GRCh37 |
| NC_000002.10:g.26267737G>A | NCBI36 |
| NG_007121.1:g.58257C>T | |
| NG_007121.2:g.58258C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380649.8:c.2178C>T (HADHA) MANE Select | ENSP00000370023.3:p.Ala726= | |
| ENST00000492433.2:c.2265C>T (HADHA) | ENSP00000438039.2:p.Ala755= | |
| ENST00000643057.1:c.*2156C>T (HADHA) | ENSP00000493761.1:n.*2156C>T | |
| ENST00000643063.1:c.*1224C>T (HADHA) | ENSP00000495353.1:n.*1224C>T | |
| ENST00000643233.1:c.*2069C>T (HADHA) | ENSP00000493880.1:n.*2069C>T | |
| ENST00000644428.1:c.*802C>T (HADHA) | ENSP00000495560.1:n.*802C>T | |
| ENST00000645274.1:c.2073C>T (HADHA) | ENSP00000493996.1:p.Ala691= | |
| ENST00000646031.1:c.1537C>T (HADHA) | ||
| ENST00000646483.1:c.2044C>T (HADHA) | ENSP00000496185.1:n.2044C>T | |
| ENST00000380649.7:c.2178C>T (HADHA) | ENSP00000370023.3:p.Ala726= | |
| ENST00000492433.1:c.723C>T (HADHA) | ENSP00000438039.1:p.Ala241= | |
| NM_000182.4:c.2178C>T (HADHA) | NP_000173.2:p.Ala726= | |
| XM_011532567.1:c.1683+4049G>A (GAREM2) | XP_011530869.1:n.1683+4049G>A | |
| XM_011532567.3:c.1683+4049G>A (GAREM2) | XP_011530869.1:n.1683+4049G>A | |
| NM_000182.5:c.2178C>T (HADHA) MANE Select | NP_000173.2:p.Ala726= |