Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.47331857_47331867del , CM000673.2:g.47331857_47331867del | GRCh38 |
| NC_000011.9:g.47353408_47353418del , CM000673.1:g.47353408_47353418del | GRCh37 |
| NC_000011.8:g.47309984_47309994del | NCBI36 |
| NG_007667.1:g.25838_25848del , LRG_386:g.25838_25848del | |
| NG_029462.1:g.67482_67492del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000545968.6:c.*6_*16del MANE Select | ENSP00000442795.1:n.*6_*16del | |
| ENST00000256993.8:c.*6_*16del | ENSP00000256993.5:n.*6_*16del | |
| ENST00000399249.6:c.*6_*16del | ENSP00000382193.2:n.*6_*16del | |
| ENST00000545968.5:c.*6_*16del | ENSP00000442795.1:n.*6_*16del | |
| NM_000256.3:c.*6_*16del , LRG_386t1:c.*6_*16del MANE Select | NP_000247.2:n.*6_*16del | |
| XM_011520117.1:c.*6_*16del | XP_011518419.1:n.*6_*16del | |
| XM_011520118.1:c.*6_*16del | XP_011518420.1:n.*6_*16del |