Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.21215721_21215722delinsCA , CM000674.2:g.21215721_21215722delinsCA | GRCh38 |
| NC_000012.11:g.21368655_21368656delinsCA , CM000674.1:g.21368655_21368656delinsCA | GRCh37 |
| NC_000012.10:g.21259922_21259923delinsCA | NCBI36 |
| NG_011745.1:g.89528_89529delinsCA , LRG_1022:g.89528_89529delinsCA |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000256958.3:c.1498-1398_1498-1397delinsCA MANE Select | ENSP00000256958.2:n.1498-1398_1498-1397de... | |
| ENST00000256958.2:c.1498-1398_1498-1397delinsCA | ENSP00000256958.2:n.1498-1398_1498-1397de... | |
| NM_006446.4:c.1498-1398_1498-1397delinsCA , LRG_1022t1:c.1498-1398_1498-1397delinsCA | NP_006437.3:n.1498-1398_1498-1397delinsCA... | |
| NM_006446.5:c.1498-1398_1498-1397delinsCA MANE Select | NP_006437.3:n.1498-1398_1498-1397delinsCA... |