Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.102846895_102846951dup , CM000674.2:g.102846895_102846951dup | GRCh38 |
| NC_000012.11:g.103240673_103240729dup , CM000674.1:g.103240673_103240729dup | GRCh37 |
| NC_000012.10:g.101764803_101764859dup | NCBI36 |
| NG_008690.1:g.75653_75709dup | |
| NG_008690.2:g.116461_116517dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000553106.6:c.914_969+1dup | ||
| ENST00000307000.7:c.899_954+1dup | ||
| ENST00000549247.6:n.673_728+1dup | ||
| ENST00000551114.2:n.576_631+1dup | ||
| ENST00000553106.5:c.914_969+1dup | ||
| ENST00000635477.1:c.74-2519_74-2463dup | ||
| ENST00000635528.1:n.429_484+1dup | ||
| NM_000277.1:c.914_969+1dup | ||
| XM_011538422.1:c.913-2519_913-2463dup | XP_011536724.1:n.913-2519_913-2463dup | |
| NM_000277.2:c.914_969+1dup | ||
| NM_001354304.1:c.914_969+1dup | ||
| NM_000277.3:c.914_969+1dup | ||
| NM_001354304.2:c.914_969+1dup |