Linked Data
gnomAD v4:
4-67932030-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.67932032del , CM000666.2:g.67932032del | GRCh38 |
| NC_000004.11:g.68797750del , CM000666.1:g.68797750del | GRCh37 |
| NC_000004.10:g.68480345del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000508048.6:c.282del MANE Select | ENSP00000426911.2:p.Trp94Ter | |
| ENST00000334830.11:c.291del | ENSP00000334611.7:p.Trp97Ter | |
| ENST00000396188.3:c.282del | ENSP00000379491.3:p.Trp94Ter | |
| ENST00000508048.5:c.282del | ENSP00000426911.2:p.Trp94Ter | |
| ENST00000513536.5:c.222del | ENSP00000427621.1:p.Trp74Ter | |
| NM_001114387.1:c.282del | NP_001107859.1:p.Trp94Ter | |
| NM_182606.3:c.291del | NP_872412.3:p.Trp97Ter | |
| NM_001114387.2:c.282del MANE Select | NP_001107859.1:p.Trp94Ter | |
| NM_182606.4:c.291del | NP_872412.3:p.Trp97Ter |