Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.21741535_21741543dup , CM000680.2:g.21741535_21741543dup | GRCh38 |
| NC_000018.9:g.19321496_19321504dup , CM000680.1:g.19321496_19321504dup | GRCh37 |
| NC_000018.8:g.17575494_17575502dup | NCBI36 |
| NG_033272.2:g.41579_41587dup , LRG_759:g.41579_41587dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261537.7:c.-49_-41dup MANE Select | ENSP00000261537.6:n.-49_-41dup | |
| ENST00000261537.6:c.-49_-41dup | ENSP00000261537.6:n.-49_-41dup | |
| ENST00000578646.5:n.168-24237_168-24229dup | ||
| NM_020774.3:c.-49_-41dup , LRG_759t1:c.-49_-41dup | NP_065825.1:n.-49_-41dup | |
| XR_935234.1:n.743_751dup | ||
| XR_935235.1:n.743_751dup | ||
| XM_017025874.1:c.-49_-41dup | XP_016881363.1:n.-49_-41dup | |
| XM_017025875.1:c.-49_-41dup | XP_016881364.1:n.-49_-41dup | |
| NM_020774.4:c.-49_-41dup MANE Select | NP_065825.1:n.-49_-41dup |