Linked Data
gnomAD v4:
7-21559110-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.21559113del , CM000669.2:g.21559113del | GRCh38 |
| NC_000007.13:g.21598731del , CM000669.1:g.21598731del | GRCh37 |
| NC_000007.12:g.21565256del | NCBI36 |
| NG_012886.2:g.20899del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000409508.8:c.692+115del MANE Select | ENSP00000475939.1:n.692+115del | |
| ENST00000328843.10:c.692+115del | ENSP00000330671.7:n.692+115del | |
| ENST00000409508.7:c.692+115del | ENSP00000475939.1:n.692+115del | |
| ENST00000620169.4:c.692+115del | ENSP00000481693.1:n.692+115del | |
| NM_001277115.1:c.692+115del | NP_001264044.1:n.692+115del | |
| NM_001277115.2:c.692+115del MANE Select | NP_001264044.1:n.692+115del |