Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215671359_215671364del , CM000663.2:g.215671359_215671364del | GRCh38 |
| NC_000001.10:g.215844701_215844706del , CM000663.1:g.215844701_215844706del | GRCh37 |
| NC_000001.9:g.213911324_213911329del | NCBI36 |
| NG_009497.1:g.757033_757038del | |
| NG_009497.2:g.757085_757090del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.13812-71_13812-66del MANE Select | ENSP00000305941.3:n.13812-71_13812-66del | |
| ENST00000674083.1:c.13812-71_13812-66del | ENSP00000501296.1:n.13812-71_13812-66del | |
| ENST00000307340.7:c.13812-71_13812-66del | ENSP00000305941.3:n.13812-71_13812-66del | |
| NM_206933.2:c.13812-71_13812-66del | NP_996816.2:n.13812-71_13812-66del | |
| NM_206933.3:c.13812-71_13812-66del | NP_996816.2:n.13812-71_13812-66del | |
| NM_206933.4:c.13812-71_13812-66del MANE Select | NP_996816.3:n.13812-71_13812-66del |