Linked Data
gnomAD v4:
21-45990481-G-GTGAGGTGAT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.45990481_45990482insTGAGGTGAT , CM000683.2:g.45990481_45990482insTGAGGTGAT | GRCh38 |
| NC_000021.8:g.47410395_47410396insTGAGGTGAT , CM000683.1:g.47410395_47410396insTGAGGTGAT | GRCh37 |
| NC_000021.7:g.46234823_46234824insTGAGGTGAT | NCBI36 |
| NG_008674.1:g.13733_13734insTGAGGTGAT , LRG_475:g.13733_13734insTGAGGTGAT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361866.8:c.1002+59_1002+60insTGAGGTGAT MANE Select | ENSP00000355180.3:n.1002+59_1002+60insTGAGGTGAT | |
| ENST00000361866.7:c.1002+59_1002+60insTGAGGTGAT | ENSP00000355180.3:n.1002+59_1002+60insTGAGGTGAT | |
| ENST00000612273.1:c.1002+59_1002+60insTGAGGTGAT | ENSP00000483630.1:n.1002+59_1002+60insTGAGGTGAT | |
| NM_001848.2:c.1002+59_1002+60insTGAGGTGAT , LRG_475t1:c.1002+59_1002+60insTGAGGTGAT | NP_001839.2:n.1002+59_1002+60insTGAGGTGAT | |
| NM_001848.3:c.1002+59_1002+60insTGAGGTGAT MANE Select | NP_001839.2:n.1002+59_1002+60insTGAGGTGAT |