Linked Data
ClinVar Variation Id:
2853549
ClinVar RCV Id:
RCV003625894
dbSNP Id:
rs1216887221
gnomAD v2:
16-68853172-TC-T
gnomAD v4:
16-68819269-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.68819273del , CM000678.2:g.68819273del | GRCh38 |
| NC_000016.9:g.68853176del , CM000678.1:g.68853176del | GRCh37 |
| NC_000016.8:g.67410677del | NCBI36 |
| NG_008021.1:g.86982del , LRG_301:g.86982del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261769.10:c.1566-7del MANE Select | ENSP00000261769.4:n.1566-7del | |
| ENST00000261769.9:c.1566-7del | ENSP00000261769.4:n.1566-7del | |
| ENST00000422392.6:c.1383-7del | ENSP00000414946.2:n.1383-7del | |
| ENST00000562836.5:n.1637-7del | ||
| ENST00000566510.5:c.*232-7del | ENSP00000458139.1:n.*232-7del | |
| ENST00000566612.5:c.1566-2728del | ENSP00000454782.1:n.1566-2728del | |
| ENST00000611625.4:c.1629-7del | ENSP00000481063.1:n.1629-7del | |
| ENST00000612417.4:c.1566-7del | ENSP00000478360.1:n.1566-7del | |
| ENST00000621016.4:c.1566-7del | ENSP00000480664.1:n.1566-7del | |
| NM_004360.3:c.1566-7del , LRG_301t1:c.1566-7del | NP_004351.1:n.1566-7del | |
| XM_011523488.1:c.831-7del | XP_011521790.1:n.831-7del | |
| XM_011523489.1:c.831-7del | XP_011521791.1:n.831-7del | |
| NM_001317184.1:c.1383-7del | NP_001304113.1:n.1383-7del | |
| NM_001317185.1:c.18-7del | NP_001304114.1:n.18-7del | |
| NM_001317186.1:c.-254-2728del | NP_001304115.1:n.-254-2728del | |
| NM_004360.4:c.1566-7del | NP_004351.1:n.1566-7del | |
| NM_004360.5:c.1566-7del MANE Select | NP_004351.1:n.1566-7del | |
| NM_001317184.2:c.1383-7del | NP_001304113.1:n.1383-7del | |
| NM_001317185.2:c.18-7del | NP_001304114.1:n.18-7del | |
| NM_001317186.2:c.-254-2728del | NP_001304115.1:n.-254-2728del |