Linked Data
gnomAD v4:
11-118312569-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.118312570del , CM000673.2:g.118312570del | GRCh38 |
| NC_000011.9:g.118183285del , CM000673.1:g.118183285del | GRCh37 |
| NC_000011.8:g.117688495del | NCBI36 |
| NG_007383.1:g.12991del , LRG_38:g.12991del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000361763.9:c.104-48del MANE Select | ENSP00000354566.4:n.104-48del | |
| ENST00000361763.8:c.104-48del | ENSP00000354566.4:n.104-48del | |
| ENST00000526146.5:n.602del | ||
| ENST00000528435.5:n.609del | ||
| ENST00000528600.1:c.86-48del | ENSP00000433975.1:n.86-48del | |
| ENST00000529713.5:n.210-48del | ||
| ENST00000531913.1:n.427del | ||
| NM_000733.3:c.104-48del , LRG_38t1:c.104-48del | NP_000724.1:n.104-48del | |
| NM_000733.4:c.104-48del MANE Select | NP_000724.1:n.104-48del |