Linked Data
MyVariant Identifiers:
chr15:g.73322680del (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322684del , CM000677.2:g.73322684del | GRCh38 |
| NC_000015.9:g.73615025del , CM000677.1:g.73615025del | GRCh37 |
| NC_000015.8:g.71402078del | NCBI36 |
| NG_009063.1:g.51585del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3413del MANE Select | ENSP00000261917.3:p.Pro1138LeufsTer? | |
| ENST00000261917.3:c.3413del | ENSP00000261917.3:p.Pro1138LeufsTer? | |
| NM_005477.2:c.3413del | NP_005468.1:p.Pro1138LeufsTer? | |
| XM_011521148.1:c.2195del | XP_011519450.1:p.Pro732LeufsTer? | |
| XM_011521148.2:c.2195del | XP_011519450.1:p.Pro732LeufsTer? | |
| NM_005477.3:c.3413del MANE Select | NP_005468.1:p.Pro1138LeufsTer? |