Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.117837159del , CM000670.2:g.117837159del | GRCh38 |
| NC_000008.10:g.118849398del , CM000670.1:g.118849398del | GRCh37 |
| NC_000008.9:g.118918579del | NCBI36 |
| NG_007455.2:g.279662del , LRG_493:g.279662del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000684189.1:n.473del | ||
| ENST00000378204.7:c.1006del MANE Select | ENSP00000367446.3:p.Val336PhefsTer23 | |
| ENST00000436216.2:c.374del | ||
| ENST00000378204.6:c.1006del | ENSP00000367446.2:p.Val336PhefsTer23 | |
| ENST00000436216.1:c.374del | ||
| ENST00000437196.1:c.74-1607del | ENSP00000407299.1:n.74-1607del | |
| NM_000127.2:c.1006del , LRG_493t1:c.1006del | NP_000118.2:p.Val336PhefsTer23 | |
| NM_000127.3:c.1006del MANE Select | NP_000118.2:p.Val336PhefsTer23 |