Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.29071139_29071140delinsTG , CM000664.2:g.29071139_29071140delinsTG | GRCh38 |
| NC_000002.11:g.29294005_29294006delinsTG , CM000664.1:g.29294005_29294006delinsTG | GRCh37 |
| NC_000002.10:g.29147509_29147510delinsTG | NCBI36 |
| NG_021427.1:g.8122_8123delinsCA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000331664.6:c.3122_3123delinsCA MANE Select | ENSP00000332809.4:p.Pro1041= | |
| ENST00000331664.5:c.3122_3123delinsCA | ENSP00000332809.4:p.Pro1041= | |
| NM_001029883.2:c.3122_3123delinsCA | NP_001025054.1:p.Pro1041= | |
| XM_011532826.1:c.3122_3123delinsCA | XP_011531128.1:p.Pro1041= | |
| XR_939901.1:n.185+1972_185+1973delinsTG | ||
| XR_939902.1:n.173+1984_173+1985delinsTG | ||
| NM_001029883.3:c.3122_3123delinsCA MANE Select | NP_001025054.1:p.Pro1041= |