Linked Data
dbSNP Id:
rs1555119652
MyVariant Identifiers:
chr11:g.118210457_118210458insAC (hg19)
chr11:g.118339742_118339743insAC (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118339743_118339744insCA , CM000673.2:g.118339743_118339744insCA | GRCh38 |
| NC_000011.9:g.118210458_118210459insCA , CM000673.1:g.118210458_118210459insCA | GRCh37 |
| NC_000011.8:g.117715668_117715669insCA | NCBI36 |
| NG_007566.1:g.400_401insCA , LRG_39:g.400_401insCA | |
| NG_009891.1:g.8002_8003insGT , LRG_37:g.8002_8003insGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000695666.1:n.925_926insGT | ||
| ENST00000695667.1:n.443_444insGT | ||
| ENST00000695668.1:n.2423_2424insGT | ||
| ENST00000300692.9:c.406+32_406+33insGT MANE Select | ENSP00000300692.4:n.406+32_406+33insGT | |
| ENST00000300692.8:c.406+32_406+33insGT | ENSP00000300692.4:n.406+32_406+33insGT | |
| ENST00000392884.2:c.275-249_275-248insGT | ENSP00000376622.2:n.275-249_275-248insGT | |
| ENST00000526561.1:n.80-249_80-248insGT | ||
| ENST00000529594.5:c.187+32_187+33insGT | ENSP00000437335.1:n.187+32_187+33insGT | |
| ENST00000534687.5:c.288-249_288-248insGT | ||
| NM_000732.4:c.406+32_406+33insGT , LRG_37t1:c.406+32_406+33insGT | NP_000723.1:n.406+32_406+33insGT | |
| NM_001040651.1:c.275-249_275-248insGT | NP_001035741.1:n.275-249_275-248insGT | |
| NM_001040651.2:c.275-249_275-248insGT | NP_001035741.1:n.275-249_275-248insGT | |
| NM_000732.6:c.406+32_406+33insGT MANE Select | NP_000723.1:n.406+32_406+33insGT |