Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652241_171652242delinsAG , CM000663.2:g.171652241_171652242delinsAG | GRCh38 |
| NC_000001.10:g.171621381_171621382delinsAG , CM000663.1:g.171621381_171621382delinsAG | GRCh37 |
| NC_000001.9:g.169888004_169888005delinsAG | NCBI36 |
| NG_008859.1:g.5392_5393delinsCT |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.370_371delinsCT MANE Select | ENSP00000037502.5:p.Leu124= | |
| ENST00000638471.1:c.130+240_130+241delinsCT | ENSP00000491206.1:n.130+240_130+241delinsCT | |
| ENST00000037502.10:c.370_371delinsCT | ENSP00000037502.5:p.Leu124= | |
| ENST00000614688.1:c.370_371delinsCT | ENSP00000478680.1:p.Leu124= | |
| NM_000261.1:c.370_371delinsCT | NP_000252.1:p.Leu124= | |
| NM_000261.2:c.370_371delinsCT MANE Select | NP_000252.1:p.Leu124= |