Linked Data
gnomAD v4:
4-52028063-C-CT
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.52028067dup , CM000666.2:g.52028067dup | GRCh38 |
| NC_000004.11:g.52894233dup , CM000666.1:g.52894233dup | GRCh37 |
| NC_000004.10:g.52588990dup | NCBI36 |
| NG_008891.1:g.15256dup , LRG_204:g.15256dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000381431.10:c.657dup MANE Select | ENSP00000370839.6:p.Val220SerfsTer2 | |
| ENST00000381431.9:c.657dup | ENSP00000370839.5:p.Val220SerfsTer2 | |
| NM_000232.4:c.657dup , LRG_204t1:c.657dup | NP_000223.1:p.Val220SerfsTer2 | |
| XM_006714049.2:c.360dup | XP_006714112.1:p.Val121SerfsTer2 | |
| XM_011534403.1:c.447dup | XP_011532705.1:p.Val150SerfsTer2 | |
| XM_011534404.1:c.360dup | XP_011532706.1:p.Val121SerfsTer2 | |
| NM_000232.5:c.657dup MANE Select | NP_000223.1:p.Val220SerfsTer2 |