Linked Data
COSMIC:
COSM5874302
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400288_18400289delinsTT , CM000670.2:g.18400288_18400289delinsTT | GRCh38 |
| NC_000008.10:g.18257798_18257799delinsTT , CM000670.1:g.18257798_18257799delinsTT | GRCh37 |
| NC_000008.9:g.18302078_18302079delinsTT | NCBI36 |
| NG_012246.1:g.14044_14045delinsTT |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000286479.4:c.285_286delinsTT MANE Select | ENSP00000286479.3:p.Pro96Ser | |
| ENST00000286479.3:c.285_286delinsTT | ENSP00000286479.3:p.Pro96Ser | |
| ENST00000520116.1:c.-57-49_-57-48delinsTT | ENSP00000428416.1:n.-57-49_-57-48delinsTT... | |
| NM_000015.2:c.285_286delinsTT | NP_000006.2:p.Pro96Ser | |
| XM_011544358.1:c.285_286delinsTT | XP_011542660.1:p.Pro96Ser | |
| XM_017012938.1:c.285_286delinsTT | XP_016868427.1:p.Pro96Ser | |
| NM_000015.3:c.285_286delinsTT MANE Select | NP_000006.2:p.Pro96Ser |