Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.215728219_215728221delinsTTG , CM000663.2:g.215728219_215728221delinsTTG | GRCh38 |
| NC_000001.10:g.215901561_215901563delinsTTG , CM000663.1:g.215901561_215901563delinsTTG | GRCh37 |
| NC_000001.9:g.213968184_213968186delinsTTG | NCBI36 |
| NG_009497.1:g.700176_700178delinsCAA | |
| NG_009497.2:g.700228_700230delinsCAA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000307340.8:c.11875_11877delinsCAA MANE Select | ENSP00000305941.3:p.Gln3959= | |
| ENST00000674083.1:c.11875_11877delinsCAA | ENSP00000501296.1:p.Gln3959= | |
| ENST00000307340.7:c.11875_11877delinsCAA | ENSP00000305941.3:p.Gln3959= | |
| NM_206933.2:c.11875_11877delinsCAA | NP_996816.2:p.Gln3959= | |
| NM_206933.3:c.11875_11877delinsCAA | NP_996816.2:p.Gln3959= | |
| NM_206933.4:c.11875_11877delinsCAA MANE Select | NP_996816.3:p.Gln3959= |