Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000018.10:g.31530960dup , CM000680.2:g.31530960dup | GRCh38 |
| NC_000018.9:g.29110923dup , CM000680.1:g.29110923dup | GRCh37 |
| NC_000018.8:g.27364921dup | NCBI36 |
| NG_007072.3:g.37719dup , LRG_397:g.37719dup |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683614.2:n.846-27dup | ||
| ENST00000683614.1:c.846-27dup | ||
| ENST00000261590.13:c.1015-27dup MANE Select | ENSP00000261590.8:n.1015-27dup | |
| ENST00000261590.12:c.1015-27dup | ENSP00000261590.8:n.1015-27dup | |
| NM_001943.3:c.1015-27dup , LRG_397t1:c.1015-27dup | NP_001934.2:n.1015-27dup | |
| NM_001943.4:c.1015-27dup | NP_001934.2:n.1015-27dup | |
| XM_024451095.1:c.481-27dup | XP_024306863.1:n.481-27dup | |
| NM_001943.5:c.1015-27dup MANE Select | NP_001934.2:n.1015-27dup |