Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.57764457G>T , CM000674.2:g.57764457G>T | GRCh38 |
| NC_000012.11:g.58158240G>T , CM000674.1:g.58158240G>T | GRCh37 |
| NC_000012.10:g.56444507G>T | NCBI36 |
| NG_007076.1:g.7737C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000713544.1:c.1138C>A | ENSP00000518840.1:p.Pro380Thr | |
| ENST00000713545.1:c.*62C>A | ENSP00000518841.1:n.*62C>A | |
| ENST00000228606.9:c.1057C>A MANE Select | ENSP00000228606.4:p.Pro353Thr | |
| ENST00000228606.8:c.1057C>A | ENSP00000228606.4:p.Pro353Thr | |
| ENST00000546567.5:c.352C>A | ENSP00000449472.1:p.Pro118Thr | |
| ENST00000547344.5:n.1196C>A | ||
| NM_000785.3:c.1057C>A | NP_000776.1:p.Pro353Thr | |
| NM_000785.4:c.1057C>A MANE Select | NP_000776.1:p.Pro353Thr |