Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.1431069_1431072delinsCTCT , CM000667.2:g.1431069_1431072delinsCTCT | GRCh38 |
| NC_000005.9:g.1431184_1431187delinsCTCT , CM000667.1:g.1431184_1431187delinsCTCT | GRCh37 |
| NC_000005.8:g.1484184_1484187delinsCTCT | NCBI36 |
| NG_015885.1:g.19357_19360delinsAGAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000270349.12:c.653+1392_653+1395delinsAGAG MANE Select | ENSP00000270349.9:n.653+1392_653+1395delinsAGAG | |
| ENST00000270349.11:c.653+1392_653+1395delinsAGAG | ENSP00000270349.9:n.653+1392_653+1395delinsAGAG | |
| NM_001044.4:c.653+1392_653+1395delinsAGAG | NP_001035.1:n.653+1392_653+1395delinsAGAG | |
| NM_001044.5:c.653+1392_653+1395delinsAGAG MANE Select | NP_001035.1:n.653+1392_653+1395delinsAGAG |