Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.38401291del , CM000685.2:g.38401291del | GRCh38 |
| NC_000023.10:g.38260544del , CM000685.1:g.38260544del | GRCh37 |
| NC_000023.9:g.38145488del | NCBI36 |
| NG_008471.1:g.53809del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000039007.5:c.403del MANE Select | ENSP00000039007.4:p.Ala135GlnfsTer? | |
| ENST00000643344.1:c.*153del | ENSP00000496606.1:n.*153del | |
| ENST00000039007.4:c.403del | ENSP00000039007.4:p.Ala135GlnfsTer? | |
| ENST00000465127.1:c.172-264830del | ENSP00000417050.1:n.172-264830del | |
| ENST00000488812.1:n.440del | ||
| NM_000531.5:c.403del | NP_000522.3:p.Ala135GlnfsTer? | |
| XM_017029556.1:c.403del | XP_016885045.1:p.Ala135GlnfsTer? | |
| NM_000531.6:c.403del MANE Select | NP_000522.3:p.Ala135GlnfsTer? |