Linked Data
ClinVar Variation Id:
223180
ClinVar RCV Id:
RCV000208801
dbSNP Id:
rs869025627
COSMIC:
COSM14386
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10142156del , CM000665.2:g.10142156del | GRCh38 |
| NC_000003.11:g.10183840del , CM000665.1:g.10183840del | GRCh37 |
| NC_000003.10:g.10158840del | NCBI36 |
| NG_008212.3:g.5522del , LRG_322:g.5522del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.309del | ENSP00000512434.1:p.Gly104AlafsTer13 | |
| ENST00000696143.1:c.309del | ENSP00000512435.1:p.Gly104AlafsTer13 | |
| ENST00000696153.1:c.309del | ENSP00000512444.1:p.Gly104AlafsTer? | |
| ENST00000256474.3:c.309del MANE Select | ENSP00000256474.3:p.Gly104AlafsTer? | |
| ENST00000256474.2:c.309del | ENSP00000256474.2:p.Gly104AlafsTer? | |
| ENST00000345392.2:c.309del | ENSP00000344757.2:p.Gly104AlafsTer14 | |
| NM_000551.3:c.309del , LRG_322t1:c.309del | NP_000542.1:p.Gly104AlafsTer? | |
| NM_198156.2:c.309del | NP_937799.1:p.Gly104AlafsTer14 | |
| XM_011534078.1:c.309del | XP_011532380.1:p.Gly104AlafsTer13 | |
| NM_001354723.1:c.309del | NP_001341652.1:p.Gly104AlafsTer13 | |
| NM_000551.4:c.309del MANE Select | NP_000542.1:p.Gly104AlafsTer? | |
| NM_001354723.2:c.309del | NP_001341652.1:p.Gly104AlafsTer13 | |
| NM_198156.3:c.309del | NP_937799.1:p.Gly104AlafsTer14 |