Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29071078_29071079delinsCG , CM000664.2:g.29071078_29071079delinsCG | GRCh38 |
| NC_000002.11:g.29293944_29293945delinsCG , CM000664.1:g.29293944_29293945delinsCG | GRCh37 |
| NC_000002.10:g.29147448_29147449delinsCG | NCBI36 |
| NG_021427.1:g.8183_8184delinsCG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.3183_3184delinsCG MANE Select | ENSP00000332809.4:p.Pro1061= | |
| ENST00000331664.5:c.3183_3184delinsCG | ENSP00000332809.4:p.Pro1061= | |
| NM_001029883.2:c.3183_3184delinsCG | NP_001025054.1:p.Pro1061= | |
| XM_011532826.1:c.3183_3184delinsCG | XP_011531128.1:p.Pro1061= | |
| XR_939901.1:n.185+1911_185+1912delinsCG | ||
| XR_939902.1:n.173+1923_173+1924delinsCG | ||
| NM_001029883.3:c.3183_3184delinsCG MANE Select | NP_001025054.1:p.Pro1061= |