Linked Data
gnomAD v2:
11-118210452-C-CACAA
gnomAD v4:
11-118339737-C-CACAA
MyVariant Identifiers:
chr11:g.118210456_118210458delinsAACACAA (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118339740_118339741insAACA , CM000673.2:g.118339740_118339741insAACA | GRCh38 |
| NC_000011.9:g.118210455_118210456insAACA , CM000673.1:g.118210455_118210456insAACA | GRCh37 |
| NC_000011.8:g.117715665_117715666insAACA | NCBI36 |
| NG_007566.1:g.397_398insAACA , LRG_39:g.397_398insAACA | |
| NG_009891.1:g.8007_8008insTTGT , LRG_37:g.8007_8008insTTGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695666.1:n.930_931insTTGT | ||
| ENST00000695667.1:n.448_449insTTGT | ||
| ENST00000695668.1:n.2428_2429insTTGT | ||
| ENST00000300692.9:c.406+37_406+38insTTGT MANE Select | ENSP00000300692.4:n.406+37_406+38insTTGT | |
| ENST00000300692.8:c.406+37_406+38insTTGT | ENSP00000300692.4:n.406+37_406+38insTTGT | |
| ENST00000392884.2:c.275-244_275-243insTTGT | ENSP00000376622.2:n.275-244_275-243insTTGT | |
| ENST00000526561.1:n.80-244_80-243insTTGT | ||
| ENST00000529594.5:c.187+37_187+38insTTGT | ENSP00000437335.1:n.187+37_187+38insTTGT | |
| ENST00000534687.5:c.288-244_288-243insTTGT | ||
| NM_000732.4:c.406+37_406+38insTTGT , LRG_37t1:c.406+37_406+38insTTGT | NP_000723.1:n.406+37_406+38insTTGT | |
| NM_001040651.1:c.275-244_275-243insTTGT | NP_001035741.1:n.275-244_275-243insTTGT | |
| NM_001040651.2:c.275-244_275-243insTTGT | NP_001035741.1:n.275-244_275-243insTTGT | |
| NM_000732.6:c.406+37_406+38insTTGT MANE Select | NP_000723.1:n.406+37_406+38insTTGT |