Linked Data
gnomAD v4:
10-110578815-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110578816del , CM000672.2:g.110578816del | GRCh38 |
| NC_000010.10:g.112338574del , CM000672.1:g.112338574del | GRCh37 |
| NC_000010.9:g.112328564del | NCBI36 |
| NG_012217.1:g.16126del , LRG_774:g.16126del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684988.1:n.562+110del | ||
| ENST00000687823.1:n.343+110del | ||
| ENST00000689932.1:n.2492+110del | ||
| ENST00000691297.1:n.562+110del | ||
| ENST00000691527.1:n.1232+110del | ||
| ENST00000692792.1:n.548+110del | ||
| ENST00000361804.5:c.429+110del MANE Select | ENSP00000354720.5:n.429+110del | |
| ENST00000361804.4:c.429+110del | ENSP00000354720.4:n.429+110del | |
| ENST00000462899.1:n.575+110del | ||
| NM_005445.3:c.429+110del , LRG_774t1:c.429+110del | NP_005436.1:n.429+110del | |
| NM_005445.4:c.429+110del MANE Select | NP_005436.1:n.429+110del |