Linked Data
dbSNP Id:
rs1565196960
gnomAD v2:
11-35282551-CG-C
gnomAD v4:
11-35261004-CG-C
MyVariant Identifiers:
chr11:g.35282552del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.35261005del , CM000673.2:g.35261005del | GRCh38 |
| NC_000011.9:g.35282552del , CM000673.1:g.35282552del | GRCh37 |
| NC_000011.8:g.35239128del | NCBI36 |
| NG_008727.1:g.163554del | |
| NG_008727.2:g.163554del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000278379.9:c.1654-40del MANE Select | ENSP00000278379.3:n.1654-40del | |
| ENST00000395750.6:c.1642-40del | ENSP00000379099.2:n.1642-40del | |
| ENST00000395753.6:c.1627-40del | ENSP00000379102.1:n.1627-40del | |
| ENST00000479543.2:n.1206-40del | ||
| ENST00000642171.1:c.*36-40del | ENSP00000495538.1:n.*36-40del | |
| ENST00000642448.1:n.1746-40del | ||
| ENST00000642769.1:c.920-40del | ||
| ENST00000643000.1:c.1627-40del | ENSP00000495164.1:n.1627-40del | |
| ENST00000643134.1:c.1654-53del | ENSP00000495188.1:n.1654-53del | |
| ENST00000643522.1:c.1420-40del | ENSP00000496375.1:n.1420-40del | |
| ENST00000644050.1:c.1627-40del | ENSP00000496123.1:n.1627-40del | |
| ENST00000644299.1:c.1627-40del | ENSP00000494669.1:n.1627-40del | |
| ENST00000644459.1:c.*146-40del | ENSP00000495861.1:n.*146-40del | |
| ENST00000644779.1:c.1765-40del | ENSP00000494258.1:n.1765-40del | |
| ENST00000644868.1:c.1716-40del | ENSP00000496760.1:n.1716-40del | |
| ENST00000645194.1:c.1627-40del | ENSP00000496093.1:n.1627-40del | |
| ENST00000645303.1:c.1669-40del | ENSP00000496667.1:n.1669-40del | |
| ENST00000645542.1:n.360-40del | ||
| ENST00000645634.1:c.1627-40del | ENSP00000493945.1:n.1627-40del | |
| ENST00000646080.1:c.1645-40del | ENSP00000494113.1:n.1645-40del | |
| ENST00000647076.1:c.395-40del | ||
| ENST00000647104.1:c.1627-40del | ENSP00000494025.1:n.1627-40del | |
| ENST00000278379.7:c.1654-40del | ENSP00000278379.3:n.1654-40del | |
| ENST00000395750.5:c.1627-40del | ENSP00000379099.1:n.1627-40del | |
| ENST00000395753.5:c.1627-40del | ENSP00000379102.1:n.1627-40del | |
| ENST00000464522.2:c.219+4522del | ENSP00000435406.1:n.219+4522del | |
| ENST00000479543.1:n.470-40del | ||
| NM_001195728.2:c.1627-40del | NP_001182657.1:n.1627-40del | |
| NM_001252652.1:c.1627-40del | NP_001239581.1:n.1627-40del | |
| NM_004171.3:c.1654-40del | NP_004162.2:n.1654-40del | |
| XM_005253067.1:c.1645-40del | XP_005253124.1:n.1645-40del | |
| XM_011520284.1:c.1702-40del | XP_011518586.1:n.1702-40del | |
| XM_011520285.1:c.1642-40del | XP_011518587.1:n.1642-40del | |
| XM_011520286.1:c.1567-40del | XP_011518588.1:n.1567-40del | |
| XM_011520287.1:c.1468-40del | XP_011518589.1:n.1468-40del | |
| XM_011520285.2:c.1642-40del | XP_011518587.1:n.1642-40del | |
| XM_017018136.1:c.1669-40del | XP_016873625.1:n.1669-40del | |
| XM_017018137.1:c.1627-40del | XP_016873626.1:n.1627-40del | |
| XM_017018138.1:c.1627-40del | XP_016873627.1:n.1627-40del | |
| XM_017018139.1:c.1420-40del | XP_016873628.1:n.1420-40del | |
| NM_004171.4:c.1654-40del MANE Select | NP_004162.2:n.1654-40del | |
| NM_001195728.3:c.1627-40del | NP_001182657.1:n.1627-40del | |
| NM_001252652.2:c.1627-40del | NP_001239581.1:n.1627-40del |