Linked Data
gnomAD v4:
15-73322910-TG-T
COSMIC:
COSM1735270
MyVariant Identifiers:
chr15:g.73615252del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322916del , CM000677.2:g.73322916del | GRCh38 |
| NC_000015.9:g.73615257del , CM000677.1:g.73615257del | GRCh37 |
| NC_000015.8:g.71402310del | NCBI36 |
| NG_009063.1:g.51354del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3182del MANE Select | ENSP00000261917.3:p.Pro1061HisfsTer? | |
| ENST00000261917.3:c.3182del | ENSP00000261917.3:p.Pro1061HisfsTer? | |
| NM_005477.2:c.3182del | NP_005468.1:p.Pro1061HisfsTer? | |
| XM_011521148.1:c.1964del | XP_011519450.1:p.Pro655HisfsTer? | |
| XM_011521148.2:c.1964del | XP_011519450.1:p.Pro655HisfsTer? | |
| NM_005477.3:c.3182del MANE Select | NP_005468.1:p.Pro1061HisfsTer? |