Linked Data
dbSNP Id:
rs1669528813
gnomAD v2:
2-26415103-AT-A
gnomAD v3:
2-26192234-AT-A
gnomAD v4:
2-26192234-AT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26192235del , CM000664.2:g.26192235del | GRCh38 |
| NC_000002.11:g.26415104del , CM000664.1:g.26415104del | GRCh37 |
| NC_000002.10:g.26268608del | NCBI36 |
| NG_007121.1:g.57386del | |
| NG_007121.2:g.57387del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380649.8:c.2000+75del (HADHA) MANE Select | ENSP00000370023.3:n.2000+75del | |
| ENST00000492433.2:c.2000+75del (HADHA) | ENSP00000438039.2:n.2000+75del | |
| ENST00000643057.1:c.*1891+75del (HADHA) | ENSP00000493761.1:n.*1891+75del | |
| ENST00000643063.1:c.*1046+75del (HADHA) | ENSP00000495353.1:n.*1046+75del | |
| ENST00000643233.1:c.*1891+75del (HADHA) | ENSP00000493880.1:n.*1891+75del | |
| ENST00000644428.1:c.*624+75del (HADHA) | ENSP00000495560.1:n.*624+75del | |
| ENST00000645274.1:c.1895+75del (HADHA) | ENSP00000493996.1:n.1895+75del | |
| ENST00000646031.1:c.1359+75del (HADHA) | ||
| ENST00000646483.1:c.1866+75del (HADHA) | ENSP00000496185.1:n.1866+75del | |
| ENST00000380649.7:c.2000+75del (HADHA) | ENSP00000370023.3:n.2000+75del | |
| ENST00000492433.1:c.458+75del (HADHA) | ENSP00000438039.1:n.458+75del | |
| NM_000182.4:c.2000+75del (HADHA) | NP_000173.2:n.2000+75del | |
| XM_011532567.1:c.1683+4920del (GAREM2) | XP_011530869.1:n.1683+4920del | |
| XM_011532567.3:c.1683+4920del (GAREM2) | XP_011530869.1:n.1683+4920del | |
| NM_000182.5:c.2000+75del (HADHA) MANE Select | NP_000173.2:n.2000+75del |