Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.116763146G= , CM000673.2:g.116763146G= | GRCh38 |
| NC_000011.9:g.116633862G= , CM000673.1:g.116633862G= | GRCh37 |
| NC_000011.8:g.116139072G= | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000260210.5:c.443C= MANE Select | ENSP00000260210.3:p.Pro148= | |
| ENST00000260210.4:c.443C= | ENSP00000260210.3:p.Pro148= | |
| ENST00000375445.7:c.443C= | ENSP00000364594.3:p.Pro148= | |
| NM_001159736.1:c.443C= | NP_001153208.1:p.Pro148= | |
| NM_032725.3:c.443C= | NP_116114.1:p.Pro148= | |
| XM_011543035.1:c.344C= | XP_011541337.1:p.Pro115= | |
| XM_011543035.2:c.344C= | XP_011541337.1:p.Pro115= | |
| NM_032725.4:c.443C= MANE Select | NP_116114.1:p.Pro148= | |
| NM_001159736.2:c.443C= | NP_001153208.1:p.Pro148= |