Linked Data
ClinVar Variation Id:
16352
ClinVar RCV Id:
RCV000017762
dbSNP Id:
rs587776836
COSMIC:
COSM723
PubMed:
PMID:11906172
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.1801945del , CM000666.2:g.1801945del | GRCh38 |
| NC_000004.11:g.1803672del , CM000666.1:g.1803672del | GRCh37 |
| NC_000004.10:g.1773470del | NCBI36 |
| NG_012632.1:g.13634del , LRG_1021:g.13634del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000340107.9:c.850del | ENSP00000339824.4:p.His284ThrfsTer10 | |
| ENST00000260795.8:c.850del | ENSP00000260795.3:p.His284ThrfsTer10 | |
| ENST00000352904.6:c.850del | ENSP00000231803.1:p.His284ThrfsTer10 | |
| ENST00000412135.7:c.838del | ENSP00000412903.3:p.His280ThrfsTer10 | |
| ENST00000440486.8:c.850del MANE Select | ENSP00000414914.2:p.His284ThrfsTer10 | |
| ENST00000481110.7:c.850del | ENSP00000420533.2:p.His284ThrfsTer10 | |
| ENST00000643463.1:n.34del | ||
| ENST00000260795.6:c.850del | ENSP00000260795.2:p.His284ThrfsTer10 | |
| ENST00000340107.8:c.850del | ENSP00000339824.4:p.His284ThrfsTer10 | |
| ENST00000352904.5:c.850del | ENSP00000231803.1:p.His284ThrfsTer10 | |
| ENST00000412135.6:c.850del | ENSP00000412903.2:p.His284ThrfsTer10 | |
| ENST00000440486.6:c.850del | ENSP00000414914.2:p.His284ThrfsTer10 | |
| ENST00000474521.1:n.226del | ||
| ENST00000481110.6:c.850del | ENSP00000420533.2:p.His284ThrfsTer10 | |
| ENST00000507588.1:c.288+22del | ENSP00000427289.1:n.288+22del | |
| ENST00000613647.4:c.850del | ENSP00000479472.1:p.His284ThrfsTer10 | |
| NM_000142.4:c.850del , LRG_1021t1:c.850del | NP_000133.1:p.His284ThrfsTer10 | |
| NM_001163213.1:c.850del , LRG_1021t2:c.850del | NP_001156685.1:p.His284ThrfsTer10 | |
| NM_022965.3:c.850del | NP_075254.1:p.His284ThrfsTer10 | |
| XM_006713868.1:c.850del | XP_006713931.1:p.His284ThrfsTer10 | |
| XM_006713869.1:c.850del | XP_006713932.1:p.His284ThrfsTer10 | |
| XM_006713870.1:c.850del | XP_006713933.1:p.His284ThrfsTer10 | |
| XM_006713871.1:c.850del | XP_006713934.1:p.His284ThrfsTer10 | |
| XM_006713872.1:c.850del | XP_006713935.1:p.His284ThrfsTer10 | |
| XM_006713873.1:c.850del | XP_006713936.1:p.His284ThrfsTer10 | |
| XM_011513420.1:c.850del | XP_011511722.1:p.His284ThrfsTer10 | |
| XM_011513422.1:c.850del | XP_011511724.1:p.His284ThrfsTer10 | |
| NM_001354809.1:c.850del | NP_001341738.1:p.His284ThrfsTer10 | |
| NM_001354810.1:c.850del | NP_001341739.1:p.His284ThrfsTer10 | |
| NR_148971.1:n.1106del | ||
| NM_001354809.2:c.850del | NP_001341738.1:p.His284ThrfsTer10 | |
| NM_001354810.2:c.850del | NP_001341739.1:p.His284ThrfsTer10 | |
| NR_148971.2:n.1125del | ||
| NM_000142.5:c.850del MANE Select | NP_000133.1:p.His284ThrfsTer10 | |
| NM_001163213.2:c.850del | NP_001156685.1:p.His284ThrfsTer10 | |
| NM_022965.4:c.850del | NP_075254.1:p.His284ThrfsTer10 |