Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.21009429_21009431delinsTAC , CM000664.2:g.21009429_21009431delinsTAC | GRCh38 |
| NC_000002.11:g.21232301_21232303delinsTAC , CM000664.1:g.21232301_21232303delinsTAC | GRCh37 |
| NC_000002.10:g.21085806_21085808delinsTAC | NCBI36 |
| NG_011793.1:g.39643_39645delinsGTA |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000233242.5:c.7437_7439delinsGTA MANE Select | ENSP00000233242.1:p.Val2479= | |
| ENST00000616098.4:c.7437_7439delinsGTA | ENSP00000477990.1:p.Val2479= | |
| NM_000384.2:c.7437_7439delinsGTA | NP_000375.2:p.Val2479= | |
| XM_011532809.1:c.5869+1302_5869+1304delinsGTA | XP_011531111.1:n.5869+1302_5869+1304delinsGTA | |
| NM_000384.3:c.7437_7439delinsGTA MANE Select | NP_000375.3:p.Val2479= |