Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764147C>G , CM000674.2:g.57764147C>G | GRCh38 |
| NC_000012.11:g.58157930C>G , CM000674.1:g.58157930C>G | GRCh37 |
| NC_000012.10:g.56444197C>G | NCBI36 |
| NG_007076.1:g.8047G>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000785.4:c.1166G>C MANE Select | NP_000776.1:p.Arg389Pro |
| ENST00000228606.9:c.1166G>C MANE Select | ENSP00000228606.4:p.Arg389Pro |
| NM_000785.3:c.1166G>C | NP_000776.1:p.Arg389Pro |
| ENST00000228606.8:c.1166G>C | ENSP00000228606.4:p.Arg389Pro |
| ENST00000546567.5:c.461G>C | ENSP00000449472.1:p.Arg154Pro |
| ENST00000547344.5:n.1305G>C | |
| ENST00000713544.1:c.1247G>C | ENSP00000518840.1:p.Arg416Pro |
| ENST00000713545.1:c.*171G>C | ENSP00000518841.1:n.*171G>C |