Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.43599573C>T , CM000677.2:g.43599573C>T | GRCh38 |
| NC_000015.9:g.43891771C>T , CM000677.1:g.43891771C>T | GRCh37 |
| NC_000015.8:g.41679063C>T | NCBI36 |
| NG_011636.1:g.24228G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000450892.7:c.*99G>A (STRC) MANE Select | ENSP00000401513.2:n.*99G>A | |
| ENST00000411560.1:n.142+40C>T (CKMT1B) | ||
| ENST00000450892.6:c.*99G>A (STRC) | ENSP00000401513.2:n.*99G>A | |
| ENST00000541030.5:c.*99G>A (STRC) | ENSP00000440413.1:n.*99G>A | |
| NM_153700.2:c.*99G>A (STRC) MANE Select | NP_714544.1:n.*99G>A | |
| XM_011521277.1:c.*99G>A (STRC) | XP_011519579.1:n.*99G>A | |
| XM_011521278.1:c.*99G>A (STRC) | XP_011519580.1:n.*99G>A | |
| XM_011521279.1:c.*99G>A (STRC) | XP_011519581.1:n.*99G>A |