Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.47283410_47283412delinsCTG , CM000679.2:g.47283410_47283412delinsCTG | GRCh38 |
| NC_000017.10:g.45360776_45360778delinsCTG , CM000679.1:g.45360776_45360778delinsCTG | GRCh37 |
| NC_000017.9:g.42715775_42715777delinsCTG | NCBI36 |
| NG_008332.2:g.34569_34571delinsCTG , LRG_481:g.34569_34571delinsCTG |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696963.1:c.222_224delinsCTG | ENSP00000513002.1:p.Asn74= | |
| ENST00000559488.7:c.222_224delinsCTG MANE Select | ENSP00000452786.2:p.Asn74= | |
| ENST00000559488.5:c.222_224delinsCTG | ENSP00000452786.1:p.Asn74= | |
| ENST00000560629.1:c.187_189delinsCTG | ||
| ENST00000571680.1:c.222_224delinsCTG | ENSP00000461626.1:p.Asn74= | |
| NM_000212.2:c.222_224delinsCTG , LRG_481t1:c.222_224delinsCTG | NP_000203.2:p.Asn74= | |
| NM_000212.3:c.222_224delinsCTG MANE Select | NP_000203.2:p.Asn74= |