Linked Data
ClinVar Variation Id:
574427
ClinVar RCV Id:
RCV000696355
dbSNP Id:
rs1559426059
CIViC:
CA891843321
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.10142124_10142141del , CM000665.2:g.10142124_10142141del | GRCh38 |
| NC_000003.11:g.10183808_10183825del , CM000665.1:g.10183808_10183825del | GRCh37 |
| NC_000003.10:g.10158808_10158825del | NCBI36 |
| NG_008212.3:g.5490_5507del , LRG_322:g.5490_5507del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696142.1:c.277_294del | ENSP00000512434.1:p.Gly93_Tyr98del | |
| ENST00000696143.1:c.277_294del | ENSP00000512435.1:p.Gly93_Tyr98del | |
| ENST00000696153.1:c.277_294del | ENSP00000512444.1:p.Gly93_Tyr98del | |
| ENST00000256474.3:c.277_294del MANE Select | ENSP00000256474.3:p.Gly93_Tyr98del | |
| ENST00000256474.2:c.277_294del | ENSP00000256474.2:p.Gly93_Tyr98del | |
| ENST00000345392.2:c.277_294del | ENSP00000344757.2:p.Gly93_Tyr98del | |
| NM_000551.3:c.277_294del , LRG_322t1:c.277_294del | NP_000542.1:p.Gly93_Tyr98del | |
| NM_198156.2:c.277_294del | NP_937799.1:p.Gly93_Tyr98del | |
| XM_011534078.1:c.277_294del | XP_011532380.1:p.Gly93_Tyr98del | |
| NM_001354723.1:c.277_294del | NP_001341652.1:p.Gly93_Tyr98del | |
| NM_000551.4:c.277_294del MANE Select | NP_000542.1:p.Gly93_Tyr98del | |
| NM_001354723.2:c.277_294del | NP_001341652.1:p.Gly93_Tyr98del | |
| NM_198156.3:c.277_294del | NP_937799.1:p.Gly93_Tyr98del |