Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.71719748_71719750delinsCCT , CM000667.2:g.71719748_71719750delinsCCT | GRCh38 |
| NC_000005.9:g.71015575_71015577delinsCCT , CM000667.1:g.71015575_71015577delinsCCT | GRCh37 |
| NC_000005.8:g.71051331_71051333delinsCCT | NCBI36 |
| NG_015988.1:g.5586_5588delinsCCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000296777.5:c.160-132_160-130delinsCCT MANE Select | ENSP00000296777.4:n.160-132_160-130delinsCCT | |
| ENST00000296777.4:c.160-132_160-130delinsCCT | ENSP00000296777.4:n.160-132_160-130delinsCCT | |
| ENST00000513096.1:n.170_172delinsCCT | ||
| NM_004291.3:c.160-132_160-130delinsCCT | NP_004282.1:n.160-132_160-130delinsCCT | |
| NM_004291.4:c.160-132_160-130delinsCCT MANE Select | NP_004282.1:n.160-132_160-130delinsCCT |