Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429979_68429980insACT , CM000663.2:g.68429979_68429980insACT | GRCh38 |
| NC_000001.10:g.68895662_68895663insACT , CM000663.1:g.68895662_68895663insACT | GRCh37 |
| NC_000001.9:g.68668250_68668251insACT | NCBI36 |
| NG_008472.1:g.24980_24981insAGT | |
| NG_008472.2:g.24980_24981insAGT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1451-53_1451-52insAGT MANE Select | ENSP00000262340.5:n.1451-53_1451-52insAGT | |
| ENST00000262340.5:c.1451-53_1451-52insAGT | ENSP00000262340.5:n.1451-53_1451-52insAGT | |
| NM_000329.2:c.1451-53_1451-52insAGT | NP_000320.1:n.1451-53_1451-52insAGT | |
| XM_017002027.1:c.1175-53_1175-52insAGT | XP_016857516.1:n.1175-53_1175-52insAGT | |
| NM_000329.3:c.1451-53_1451-52insAGT MANE Select | NP_000320.1:n.1451-53_1451-52insAGT |