Linked Data
gnomAD v4:
7-152660660-TA-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.152660663del , CM000669.2:g.152660663del | GRCh38 |
| NC_000007.13:g.152357748del , CM000669.1:g.152357748del | GRCh37 |
| NC_000007.12:g.151988681del | NCBI36 |
| NG_027988.1:g.20505del | |
| NG_027988.2:g.20505del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000698506.1:c.-47-11298del | ENSP00000513758.1:n.-47-11298del | |
| ENST00000698507.1:n.229del | ||
| ENST00000359321.2:c.121+40del MANE Select | ENSP00000352271.1:n.121+40del | |
| ENST00000359321.1:c.121+40del | ENSP00000352271.1:n.121+40del | |
| ENST00000495707.1:n.143+40del | ||
| NM_005431.1:c.121+40del | NP_005422.1:n.121+40del | |
| NM_005431.2:c.121+40del MANE Select | NP_005422.1:n.121+40del |