Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.38396821_38396822delinsAG , CM000671.2:g.38396821_38396822delinsAG | GRCh38 |
| NC_000009.11:g.38396818_38396819delinsAG , CM000671.1:g.38396818_38396819delinsAG | GRCh37 |
| NC_000009.10:g.38386818_38386819delinsAG | NCBI36 |
| NG_012253.1:g.9117_9118delinsAG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000377698.4:c.1073_1074delinsAG MANE Select | ENSP00000366927.3:p.Gln358= | |
| ENST00000377698.3:c.1073_1074delinsAG | ENSP00000366927.3:p.Gln358= | |
| NM_000692.4:c.1073_1074delinsAG | NP_000683.3:p.Gln358= | |
| XM_011517802.1:c.1073_1074delinsAG | XP_011516104.1:p.Gln358= | |
| XM_011517802.2:c.1073_1074delinsAG | XP_011516104.1:p.Gln358= | |
| NM_000692.5:c.1073_1074delinsAG MANE Select | NP_000683.3:p.Gln358= |