Linked Data
gnomAD v4:
10-80275113-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000010.11:g.80275115del , CM000672.2:g.80275115del | GRCh38 |
| NC_000010.10:g.82034871del , CM000672.1:g.82034871del | GRCh37 |
| NC_000010.9:g.82024851del | NCBI36 |
| NG_008083.1:g.19565del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000372213.8:c.854del MANE Select | ENSP00000361287.3:p.Lys285ArgfsTer6 | |
| ENST00000372213.7:c.854del | ENSP00000361287.3:p.Lys285ArgfsTer6 | |
| ENST00000480845.1:n.86del | ||
| ENST00000485270.5:n.366del | ||
| NM_000429.2:c.854del | NP_000420.1:p.Lys285ArgfsTer6 | |
| XM_005269842.3:c.854del | XP_005269899.1:p.Lys285ArgfsTer6 | |
| XM_005269843.3:c.731del | XP_005269900.1:p.Lys244ArgfsTer6 | |
| NM_000429.3:c.854del MANE Select | NP_000420.1:p.Lys285ArgfsTer6 |