Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.37966198_37966199del , CM000670.2:g.37966198_37966199del | GRCh38 |
| NC_000008.10:g.37823716_37823717del , CM000670.1:g.37823716_37823717del | GRCh37 |
| NC_000008.9:g.37942873_37942874del | NCBI36 |
| NG_011936.1:g.5469_5470del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000345060.5:c.272_273del MANE Select | ENSP00000343782.3:p.Val91AlafsTer? | |
| ENST00000520341.2:n.400_401del | ||
| ENST00000345060.4:c.272_273del | ENSP00000343782.3:p.Val91AlafsTer? | |
| ENST00000614635.1:c.272_273del | ENSP00000480325.1:p.Val91AlafsTer? | |
| NM_000025.2:c.272_273del | NP_000016.1:p.Val91AlafsTer? | |
| NM_000025.3:c.272_273del MANE Select | NP_000016.1:p.Val91AlafsTer? |