Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.108687482del , CM000685.2:g.108687482del | GRCh38 |
| NC_000023.10:g.107930712del , CM000685.1:g.107930712del | GRCh37 |
| NC_000023.9:g.107817368del | NCBI36 |
| NG_011977.1:g.252559del | |
| NG_011977.2:g.252559del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000328300.11:c.4316del | ||
| ENST00000361603.7:c.4298del | ||
| ENST00000510690.2:n.810del | ||
| ENST00000328300.10:c.4316del | ||
| ENST00000361603.6:c.4298del | ||
| ENST00000489230.1:n.719del | ||
| ENST00000515658.1:c.112del | ||
| NM_000495.4:c.4298del | ||
| NM_033380.2:c.4316del | ||
| XM_005262070.2:c.4307del | ||
| XM_006724616.2:c.4316del | ||
| XM_011530849.1:c.3992del | ||
| XM_011530851.1:c.1889del | ||
| XM_011530849.2:c.4331del | ||
| XM_017029259.2:c.4322del | ||
| XM_017029260.1:c.4313del | ||
| XM_017029263.2:c.2651del | ||
| NM_000495.5:c.4298del | ||
| NM_033380.3:c.4316del |