Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.68429985_68429986insAGA , CM000663.2:g.68429985_68429986insAGA | GRCh38 |
| NC_000001.10:g.68895668_68895669insAGA , CM000663.1:g.68895668_68895669insAGA | GRCh37 |
| NC_000001.9:g.68668256_68668257insAGA | NCBI36 |
| NG_008472.1:g.24974_24975insTCT | |
| NG_008472.2:g.24974_24975insTCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000262340.6:c.1451-59_1451-58insTCT MANE Select | ENSP00000262340.5:n.1451-59_1451-58insTCT | |
| ENST00000262340.5:c.1451-59_1451-58insTCT | ENSP00000262340.5:n.1451-59_1451-58insTCT | |
| NM_000329.2:c.1451-59_1451-58insTCT | NP_000320.1:n.1451-59_1451-58insTCT | |
| XM_017002027.1:c.1175-59_1175-58insTCT | XP_016857516.1:n.1175-59_1175-58insTCT | |
| NM_000329.3:c.1451-59_1451-58insTCT MANE Select | NP_000320.1:n.1451-59_1451-58insTCT |