Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.88732547A= , CM000678.2:g.88732547A= | GRCh38 |
| NC_000016.9:g.88798955A= , CM000678.1:g.88798955A= | GRCh37 |
| NC_000016.8:g.87326456A= | NCBI36 |
| NG_042229.1:g.57674T= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301015.14:c.2791-12T= (PIEZO1) MANE Select | ENSP00000301015.9:n.2791-12T= | |
| ENST00000301015.13:c.2791-12T= (PIEZO1) | ENSP00000301015.9:n.2791-12T= | |
| ENST00000490756.1:n.375-12T= (PIEZO1) | ||
| NM_001142864.2:c.2791-12T= (PIEZO1) | NP_001136336.2:n.2791-12T= | |
| NM_001142864.3:c.2791-12T= (PIEZO1) | NP_001136336.2:n.2791-12T= | |
| NR_103774.1:n.269+1099A= (HSALR1) | ||
| NM_001142864.4:c.2791-12T= (PIEZO1) MANE Select | NP_001136336.2:n.2791-12T= |