Linked Data
gnomAD v4:
15-73323099-TG-T
COSMIC:
COSM1374433
MyVariant Identifiers:
chr15:g.73615441del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73323104del , CM000677.2:g.73323104del | GRCh38 |
| NC_000015.9:g.73615445del , CM000677.1:g.73615445del | GRCh37 |
| NC_000015.8:g.71402498del | NCBI36 |
| NG_009063.1:g.51165del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.2993del MANE Select | ENSP00000261917.3:p.Pro998HisfsTer20 | |
| ENST00000261917.3:c.2993del | ENSP00000261917.3:p.Pro998HisfsTer20 | |
| NM_005477.2:c.2993del | NP_005468.1:p.Pro998HisfsTer20 | |
| XM_011521148.1:c.1775del | XP_011519450.1:p.Pro592HisfsTer20 | |
| XM_011521148.2:c.1775del | XP_011519450.1:p.Pro592HisfsTer20 | |
| NM_005477.3:c.2993del MANE Select | NP_005468.1:p.Pro998HisfsTer20 |