Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.48583172dup , CM000665.2:g.48583172dup | GRCh38 |
| NC_000003.11:g.48620605dup , CM000665.1:g.48620605dup | GRCh37 |
| NC_000003.10:g.48595609dup | NCBI36 |
| NG_007065.1:g.17083dup , LRG_286:g.17083dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000681320.1:c.4439dup | ||
| ENST00000328333.12:c.4439dup | ||
| ENST00000487017.5:n.356dup | ||
| NM_000094.3:c.4439dup , LRG_286t1:c.4439dup | ||
| XM_011533336.1:c.4466dup | ||
| XM_011533337.1:c.4439dup | ||
| XM_011533338.1:c.4466dup | ||
| XM_011533339.1:c.4466dup | ||
| XM_011533340.1:c.4466dup | ||
| XM_011533341.1:c.4466dup | ||
| XM_011533342.1:c.4466dup | ||
| XR_940369.1:n.4502dup | ||
| XR_940370.1:n.4502dup | ||
| XR_940371.1:n.4502dup | ||
| XR_940372.1:n.4502dup | ||
| XR_940373.1:n.4502dup | ||
| XR_940374.1:n.4502dup | ||
| XR_940375.1:n.4502dup | ||
| XM_017005688.1:c.4439dup | ||
| XM_017005689.1:c.4439dup | ||
| XM_017005690.1:c.4439dup | ||
| XM_017005691.1:c.4439dup | ||
| XM_017005692.1:c.4439dup | ||
| XR_001740003.1:n.4475dup | ||
| XR_001740004.1:n.4475dup | ||
| XR_001740005.1:n.4475dup | ||
| XR_001740006.1:n.4475dup | ||
| XR_001740007.1:n.4475dup | ||
| XR_001740008.1:n.4475dup | ||
| XR_001740009.1:n.4475dup | ||
| NM_000094.4:c.4439dup |