Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88738270G>T , CM000678.2:g.88738270G>T | GRCh38 |
| NC_000016.9:g.88804678G>T , CM000678.1:g.88804678G>T | GRCh37 |
| NC_000016.8:g.87332179G>T | NCBI36 |
| NG_042229.1:g.51951C>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000301015.14:c.805C>A (PIEZO1) MANE Select | ENSP00000301015.9:p.Pro269Thr | |
| ENST00000301015.13:c.805C>A (PIEZO1) | ENSP00000301015.9:p.Pro269Thr | |
| NM_001142864.2:c.805C>A (PIEZO1) | NP_001136336.2:p.Pro269Thr | |
| NM_001142864.3:c.805C>A (PIEZO1) | NP_001136336.2:p.Pro269Thr | |
| NR_103774.1:n.719G>T (HSALR1) | ||
| NM_001142864.4:c.805C>A (PIEZO1) MANE Select | NP_001136336.2:p.Pro269Thr |