Linked Data
gnomAD v4:
6-31270322-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000006.12:g.31270324del , CM000668.2:g.31270324del | GRCh38 |
| NC_000006.11:g.31238101del , CM000668.1:g.31238101del | GRCh37 |
| NC_000006.10:g.31346080del | NCBI36 |
| NG_029422.2:g.6809del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376228.10:c.782del MANE Select | ENSP00000365402.5:p.Gly261GlufsTer? | |
| ENST00000376228.9:c.782del | ENSP00000365402.5:p.Gly261GlufsTer? | |
| ENST00000376237.8:c.*369del | ENSP00000365412.4:n.*369del | |
| ENST00000383329.7:c.782del | ENSP00000372819.3:p.Gly261GlufsTer? | |
| ENST00000415537.1:c.673del | ||
| ENST00000470363.5:n.100del | ||
| ENST00000487245.5:n.1141del | ||
| ENST00000495835.1:n.971del | ||
| NM_002117.5:c.782del | NP_002108.4:p.Gly261GlufsTer? | |
| NM_002117.6:c.782del MANE Select | NP_002108.4:p.Gly261GlufsTer? |