MyVariant.info:
GRCh38
chr3:g.33058085_33058087del
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.33058086_33058088del , CM000665.2:g.33058086_33058088del | GRCh38 |
| NC_000003.11:g.33099578_33099580del , CM000665.1:g.33099578_33099580del | GRCh37 |
| NC_000003.10:g.33074582_33074584del | NCBI36 |
| NG_009005.1:g.44116_44118del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307363.10:c.733+2_733+4del MANE Select | ENSP00000306920.4:n.733+2_733+4del | |
| ENST00000307363.9:c.733+2_733+4del | ENSP00000306920.4:n.733+2_733+4del | |
| ENST00000307377.12:c.341-4538_341-4536del | ENSP00000305920.8:n.341-4538_341-4536del | |
| ENST00000399402.7:c.643+2_643+4del | ENSP00000382333.2:n.643+2_643+4del | |
| ENST00000415454.1:c.256+2_256+4del | ENSP00000411813.1:n.256+2_256+4del | |
| ENST00000438227.1:c.*225+2_*225+4del | ENSP00000401250.1:n.*225+2_*225+4del | |
| ENST00000446732.5:c.*176+2_*176+4del | ENSP00000407365.1:n.*176+2_*176+4del | |
| ENST00000482097.5:n.109-4538_109-4536del | ||
| ENST00000485698.5:n.137-4538_137-4536del | ||
| ENST00000498537.5:n.133-4538_133-4536del | ||
| NM_000404.2:c.733+2_733+4del | NP_000395.2:n.733+2_733+4del | |
| NM_000404.3:c.733+2_733+4del | NP_000395.2:n.733+2_733+4del | |
| NM_001079811.1:c.643+2_643+4del | NP_001073279.1:n.643+2_643+4del | |
| NM_001079811.2:c.643+2_643+4del | NP_001073279.1:n.643+2_643+4del | |
| NM_001135602.1:c.341-4538_341-4536del | NP_001129074.1:n.341-4538_341-4536del | |
| NM_001135602.2:c.341-4538_341-4536del | NP_001129074.1:n.341-4538_341-4536del | |
| NM_001317040.1:c.877+2_877+4del | NP_001303969.1:n.877+2_877+4del | |
| NM_000404.4:c.733+2_733+4del MANE Select | NP_000395.3:n.733+2_733+4del | |
| NM_001079811.3:c.643+2_643+4del | NP_001073279.2:n.643+2_643+4del | |
| NM_001135602.3:c.341-4538_341-4536del | NP_001129074.2:n.341-4538_341-4536del | |
| NM_001317040.2:c.877+2_877+4del | NP_001303969.2:n.877+2_877+4del | |
| NM_001393580.1:c.733+2_733+4del | NP_001380509.1:n.733+2_733+4del |