Linked Data
gnomAD v4:
15-73322901-CTGGGGTGG-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000015.10:g.73322907_73322914del , CM000677.2:g.73322907_73322914del | GRCh38 |
| NC_000015.9:g.73615248_73615255del , CM000677.1:g.73615248_73615255del | GRCh37 |
| NC_000015.8:g.71402301_71402308del | NCBI36 |
| NG_009063.1:g.51356_51363del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261917.4:c.3184_3191del MANE Select | ENSP00000261917.3:p.Pro1062GlyfsTer? | |
| ENST00000261917.3:c.3184_3191del | ENSP00000261917.3:p.Pro1062GlyfsTer? | |
| NM_005477.2:c.3184_3191del | NP_005468.1:p.Pro1062GlyfsTer? | |
| XM_011521148.1:c.1966_1973del | XP_011519450.1:p.Pro656GlyfsTer? | |
| XM_011521148.2:c.1966_1973del | XP_011519450.1:p.Pro656GlyfsTer? | |
| NM_005477.3:c.3184_3191del MANE Select | NP_005468.1:p.Pro1062GlyfsTer? |