Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.154903513del , CM000685.2:g.154903513del | GRCh38 |
| NC_000023.10:g.154131788del , CM000685.1:g.154131788del | GRCh37 |
| NC_000023.9:g.153784982del | NCBI36 |
| NG_011403.1:g.124214del | |
| NG_011403.2:g.124214del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360256.9:c.5998+396del MANE Select | ENSP00000353393.4:n.5998+396del | |
| ENST00000360256.8:c.5998+396del | ENSP00000353393.4:n.5998+396del | |
| NM_000132.3:c.5998+396del | NP_000123.1:n.5998+396del | |
| XM_011531126.1:c.5893+396del | XP_011529428.1:n.5893+396del | |
| NM_000132.4:c.5998+396del MANE Select | NP_000123.1:n.5998+396del |