Linked Data
gnomAD v4:
17-43755713-CG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.43755715del , CM000679.2:g.43755715del | GRCh38 |
| NC_000017.10:g.41833083del , CM000679.1:g.41833083del | GRCh37 |
| NC_000017.9:g.39188609del | NCBI36 |
| NG_008078.2:g.8075del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000301691.3:c.270del MANE Select | ENSP00000301691.1:p.Asp91MetfsTer? | |
| ENST00000301691.2:c.270del | ENSP00000301691.1:p.Asp91MetfsTer? | |
| NM_025237.2:c.270del | NP_079513.1:p.Asp91MetfsTer? | |
| NM_025237.3:c.270del MANE Select | NP_079513.1:p.Asp91MetfsTer? |