Linked Data
dbSNP Id:
rs2135979564
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128891593del , CM000673.2:g.128891593del | GRCh38 |
| NC_000011.9:g.128761488del , CM000673.1:g.128761488del | GRCh37 |
| NC_000011.8:g.128266698del | NCBI36 |
| NG_023406.2:g.5176del , LRG_333:g.5176del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000529694.6:c.-139del MANE Select | ENSP00000433295.1:n.-139del | |
| ENST00000338350.4:c.-228del | ENSP00000339960.4:n.-228del | |
| ENST00000529694.5:c.-139del | ENSP00000433295.1:n.-139del | |
| NM_000890.3:c.-139del , LRG_333t1:c.-139del | NP_000881.3:n.-139del | |
| NM_000890.4:c.-139del | NP_000881.3:n.-139del | |
| NM_001354169.1:c.-228del | NP_001341098.1:n.-228del | |
| NM_000890.5:c.-139del MANE Select | NP_000881.3:n.-139del | |
| NM_001354169.2:c.-228del | NP_001341098.1:n.-228del |