Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.38363207_38363210delinsTATC , CM000682.2:g.38363207_38363210delinsTATC | GRCh38 |
| NC_000020.10:g.36991861_36991864delinsTATC , CM000682.1:g.36991861_36991864delinsTATC | GRCh37 |
| NC_000020.9:g.36425275_36425278delinsTATC | NCBI36 |
| NG_034239.1:g.21797_21800delinsTATC |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000217407.3:c.653-768_653-765delinsTATC MANE Select | ENSP00000217407.2:n.653-768_653-765delinsTATC | |
| ENST00000217407.2:c.653-768_653-765delinsTATC | ENSP00000217407.2:n.653-768_653-765delinsTATC | |
| NM_004139.4:c.653-768_653-765delinsTATC | NP_004130.2:n.653-768_653-765delinsTATC | |
| NM_004139.5:c.653-768_653-765delinsTATC MANE Select | NP_004130.2:n.653-768_653-765delinsTATC |