Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37966159_37966176delinsGGCCAGTGGCCAGTCAGC , CM000670.2:g.37966159_37966176delinsGGCCAGTGGCCAGTCAGC | GRCh38 |
| NC_000008.10:g.37823677_37823694delinsGGCCAGTGGCCAGTCAGC , CM000670.1:g.37823677_37823694delinsGGCCAGTGGCCAGTCAGC | GRCh37 |
| NC_000008.9:g.37942834_37942851delinsGGCCAGTGGCCAGTCAGC | NCBI36 |
| NG_011936.1:g.5491_5508delinsGCTGACTGGCCACTGGCC |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000345060.5:c.294_311delinsGCTGACTGGCCACTGGCC MANE Select | ENSP00000343782.3:p.Ala98= | |
| ENST00000520341.2:n.422_439delinsGCTGACTGGCCACTGGCC | ||
| ENST00000345060.4:c.294_311delinsGCTGACTGGCCACTGGCC | ENSP00000343782.3:p.Ala98= | |
| ENST00000614635.1:c.294_311delinsGCTGACTGGCCACTGGCC | ENSP00000480325.1:p.Ala98= | |
| NM_000025.2:c.294_311delinsGCTGACTGGCCACTGGCC | NP_000016.1:p.Ala98= | |
| NM_000025.3:c.294_311delinsGCTGACTGGCCACTGGCC MANE Select | NP_000016.1:p.Ala98= |