Linked Data
gnomAD v4:
10-110812385-G-GT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.110812385_110812386insT , CM000672.2:g.110812385_110812386insT | GRCh38 |
| NC_000010.10:g.112572143_112572144insT , CM000672.1:g.112572143_112572144insT | GRCh37 |
| NC_000010.9:g.112562133_112562134insT | NCBI36 |
| NG_021177.1:g.172989_172990insT , LRG_382:g.172989_172990insT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000369519.4:c.1988_1989insT MANE Select | ENSP00000358532.3:p.Ser665LeufsTer4 | |
| ENST00000369519.3:c.1988_1989insT | ENSP00000358532.3:p.Ser665LeufsTer4 | |
| NM_001134363.2:c.1988_1989insT | NP_001127835.2:p.Ser665LeufsTer4 | |
| XM_011539697.1:c.1604_1605insT | XP_011537999.1:p.Ser537LeufsTer4 | |
| XM_017016103.2:c.1823_1824insT | XP_016871592.1:p.Ser610LeufsTer4 | |
| XM_017016104.2:c.1604_1605insT | XP_016871593.1:p.Ser537LeufsTer4 | |
| NM_001134363.3:c.1988_1989insT MANE Select | NP_001127835.2:p.Ser665LeufsTer4 |