Linked Data
gnomAD v4:
22-43928863-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.43928865del , CM000684.2:g.43928865del | GRCh38 |
| NC_000022.10:g.44324745del , CM000684.1:g.44324745del | GRCh37 |
| NC_000022.9:g.42656078del | NCBI36 |
| NG_008631.1:g.10127del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000216180.8:c.462del MANE Select | ENSP00000216180.3:p.Ile155SerfsTer15 | |
| ENST00000216180.7:c.462del | ENSP00000216180.3:p.Ile155SerfsTer15 | |
| ENST00000406117.6:c.*94del | ENSP00000384668.2:n.*94del | |
| ENST00000423180.2:c.450del | ENSP00000397987.2:p.Ile151SerfsTer15 | |
| ENST00000478713.1:n.496del | ||
| NM_025225.2:c.462del | NP_079501.2:p.Ile155SerfsTer15 | |
| NM_025225.3:c.462del MANE Select | NP_079501.2:p.Ile155SerfsTer15 |