Linked Data
dbSNP Id:
rs1308115081
gnomAD v2:
2-26424216-TG-T
gnomAD v3:
2-26201347-TG-T
gnomAD v4:
2-26201347-TG-T
MyVariant Identifiers:
chr2:g.26424217del (hg19)
chr2:g.26201349del (hg38)
chr2:g.26201348del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.26201350del , CM000664.2:g.26201350del | GRCh38 |
| NC_000002.11:g.26424219del , CM000664.1:g.26424219del | GRCh37 |
| NC_000002.10:g.26277723del | NCBI36 |
| NG_007121.1:g.48273del | |
| NG_007121.2:g.48274del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380649.8:c.1221-28del (HADHA) MANE Select | ENSP00000370023.3:n.1221-28del | |
| ENST00000492433.2:c.1221-28del (HADHA) | ENSP00000438039.2:n.1221-28del | |
| ENST00000643057.1:c.*1112-28del (HADHA) | ENSP00000493761.1:n.*1112-28del | |
| ENST00000643063.1:c.*267-28del (HADHA) | ENSP00000495353.1:n.*267-28del | |
| ENST00000643233.1:c.*1112-28del (HADHA) | ENSP00000493880.1:n.*1112-28del | |
| ENST00000644428.1:c.1221-28del (HADHA) | ENSP00000495560.1:n.1221-28del | |
| ENST00000645274.1:c.1116-28del (HADHA) | ENSP00000493996.1:n.1116-28del | |
| ENST00000646031.1:c.580-28del (HADHA) | ||
| ENST00000646483.1:c.1087-28del (HADHA) | ENSP00000496185.1:n.1087-28del | |
| ENST00000380649.7:c.1221-28del (HADHA) | ENSP00000370023.3:n.1221-28del | |
| NM_000182.4:c.1221-28del (HADHA) | NP_000173.2:n.1221-28del | |
| XM_011532567.1:c.1684-883del (GAREM2) | XP_011530869.1:n.1684-883del | |
| XM_011532567.3:c.1684-883del (GAREM2) | XP_011530869.1:n.1684-883del | |
| NM_000182.5:c.1221-28del (HADHA) MANE Select | NP_000173.2:n.1221-28del |