Linked Data
dbSNP Id:
rs1375654397
gnomAD v2:
16-30997501-ACCAT-A
gnomAD v3:
16-30986180-ACCAT-A
gnomAD v4:
16-30986180-ACCAT-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.30986185_30986188del , CM000678.2:g.30986185_30986188del | GRCh38 |
| NC_000016.9:g.30997506_30997509del , CM000678.1:g.30997506_30997509del | GRCh37 |
| NC_000016.8:g.30905007_30905010del | NCBI36 |
| NG_012346.1:g.5988_5991del | |
| NG_052948.1:g.33892_33895del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000297679.10:c.303_306del MANE Select | ENSP00000297679.5:p.Ile101MetfsTer11 | |
| ENST00000262520.10:c.303_306del | ENSP00000262520.6:p.Ile101MetfsTer11 | |
| ENST00000297679.9:c.303_306del | ENSP00000297679.5:p.Ile101MetfsTer11 | |
| ENST00000562932.5:c.426_429del | ENSP00000459852.1:p.Ile142MetfsTer11 | |
| ENST00000574447.1:c.303_306del | ENSP00000459689.1:p.Ile101MetfsTer11 | |
| NM_001142777.1:c.303_306del | NP_001136249.1:p.Ile101MetfsTer11 | |
| NM_001142778.1:c.303_306del | NP_001136250.1:p.Ile101MetfsTer11 | |
| NM_025193.3:c.303_306del | NP_079469.2:p.Ile101MetfsTer11 | |
| XM_005255601.3:c.303_306del | XP_005255658.2:p.Ile101MetfsTer11 | |
| XM_011545960.1:c.303_306del | XP_011544262.1:p.Ile101MetfsTer11 | |
| XM_011545961.1:c.303_306del | XP_011544263.1:p.Ile101MetfsTer11 | |
| XM_011545962.1:c.303_306del | XP_011544264.1:p.Ile101MetfsTer11 | |
| XM_011545960.2:c.303_306del | XP_011544262.1:p.Ile101MetfsTer11 | |
| XM_011545962.2:c.303_306del | XP_011544264.1:p.Ile101MetfsTer11 | |
| XM_017023732.1:c.303_306del | XP_016879221.1:p.Ile101MetfsTer11 | |
| NM_025193.4:c.303_306del MANE Select | NP_079469.2:p.Ile101MetfsTer11 | |
| NM_001142777.2:c.303_306del | NP_001136249.1:p.Ile101MetfsTer11 | |
| NM_001142778.2:c.303_306del | NP_001136250.1:p.Ile101MetfsTer11 |