Linked Data
gnomAD v4:
22-43928756-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928758del , CM000684.2:g.43928758del | GRCh38 |
| NC_000022.10:g.44324638del , CM000684.1:g.44324638del | GRCh37 |
| NC_000022.9:g.42655971del | NCBI36 |
| NG_008631.1:g.10020del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.421-66del MANE Select | ENSP00000216180.3:n.421-66del | |
| ENST00000216180.7:c.421-66del | ENSP00000216180.3:n.421-66del | |
| ENST00000406117.6:c.*53-66del | ENSP00000384668.2:n.*53-66del | |
| ENST00000423180.2:c.409-66del | ENSP00000397987.2:n.409-66del | |
| ENST00000478713.1:n.455-66del | ||
| NM_025225.2:c.421-66del | NP_079501.2:n.421-66del | |
| NM_025225.3:c.421-66del MANE Select | NP_079501.2:n.421-66del |