Linked Data
gnomAD v4:
14-28767626-TGGACGGGGCTAAAGC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.28767634_28767648del , CM000676.2:g.28767634_28767648del | GRCh38 |
| NC_000014.8:g.29236840_29236854del , CM000676.1:g.29236840_29236854del | GRCh37 |
| NC_000014.7:g.28306591_28306605del | NCBI36 |
| NG_009367.1:g.5554_5568del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000706482.1:c.355_369del | ENSP00000516406.1:p.Ala119_Gly123del | |
| ENST00000313071.7:c.355_369del MANE Select | ENSP00000339004.3:p.Ala119_Gly123del | |
| ENST00000313071.6:c.355_369del | ENSP00000339004.3:p.Ala119_Gly123del | |
| NM_005249.4:c.355_369del | NP_005240.3:p.Ala119_Gly123del | |
| NM_005249.5:c.355_369del MANE Select | NP_005240.3:p.Ala119_Gly123del |