Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652085_171652086delinsTC , CM000663.2:g.171652085_171652086delinsTC | GRCh38 |
| NC_000001.10:g.171621225_171621226delinsTC , CM000663.1:g.171621225_171621226delinsTC | GRCh37 |
| NC_000001.9:g.169887848_169887849delinsTC | NCBI36 |
| NG_008859.1:g.5548_5549delinsGA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.526_527delinsGA MANE Select | ENSP00000037502.5:p.Glu176= | |
| ENST00000638471.1:c.130+396_130+397delinsGA | ENSP00000491206.1:n.130+396_130+397delinsGA | |
| ENST00000037502.10:c.526_527delinsGA | ENSP00000037502.5:p.Glu176= | |
| ENST00000614688.1:c.526_527delinsGA | ENSP00000478680.1:p.Glu176= | |
| NM_000261.1:c.526_527delinsGA | NP_000252.1:p.Glu176= | |
| NM_000261.2:c.526_527delinsGA MANE Select | NP_000252.1:p.Glu176= |