Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.22812203G>A , CM000677.2:g.22812203G>A | GRCh38 |
| NC_000015.9:g.23060865C>T , CM000677.1:g.23060865C>T | GRCh37 |
| NC_000015.8:g.20612306C>T | NCBI36 |
| NG_009056.1:g.30979G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_144599.5:c.267G>A MANE Select | NP_653200.2:p.Ala89= |
| ENST00000337435.9:c.267G>A MANE Select | ENSP00000337452.4:p.Ala89= |
| NM_001142275.1:c.42G>A | NP_001135747.1:p.Ala14= |
| NM_144599.4:c.267G>A | NP_653200.2:p.Ala89= |
| ENST00000337435.8:c.267G>A | ENSP00000337452.4:p.Ala89= |
| ENST00000437912.6:c.42G>A | ENSP00000393962.2:p.Ala14= |
| ENST00000557930.1:c.111G>A | ENSP00000453797.1:p.Ala37= |
| ENST00000559448.5:c.157G>A | |
| ENST00000560069.5:n.120G>A | |
| ENST00000561183.5:c.42G>A | ENSP00000453722.1:p.Ala14= |