Linked Data
ClinVar Variation Id:
341103
ClinVar RCV Id:
RCV000284617
dbSNP Id:
rs886057353
gnomAD v4:
22-29696065-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.29696066del , CM000684.2:g.29696066del | GRCh38 |
| NC_000022.10:g.30092055del , CM000684.1:g.30092055del | GRCh37 |
| NC_000022.9:g.28422055del | NCBI36 |
| NG_009057.1:g.97511del , LRG_511:g.97511del |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000338641.10:c.*1264del MANE Select | ENSP00000344666.5:n.*1264del | |
| ENST00000672461.1:c.*501+823del | ENSP00000500919.1:n.*501+823del | |
| ENST00000672896.1:c.*1324del | ENSP00000500117.1:n.*1324del | |
| ENST00000338641.8:c.*1264del | ENSP00000344666.4:n.*1264del | |
| ENST00000361452.8:c.*1324del | ENSP00000354897.4:n.*1324del | |
| ENST00000413209.6:c.*1264del | ENSP00000409921.2:n.*1264del | |
| NM_000268.3:c.*1264del , LRG_511t1:c.*1264del | NP_000259.1:n.*1264del | |
| NM_016418.5:c.*1324del , LRG_511t2:c.*1324del | NP_057502.2:n.*1324del | |
| NM_181828.2:c.*1324del | NP_861966.1:n.*1324del | |
| NM_181829.2:c.*1324del | NP_861967.1:n.*1324del | |
| NM_181830.2:c.*1324del | NP_861968.1:n.*1324del | |
| NM_181832.2:c.*1339del | NP_861970.1:n.*1339del | |
| NM_181833.2:c.*1264del | NP_861971.1:n.*1264del | |
| NR_156186.1:n.3611del | ||
| XM_017028810.1:c.*1324del | XP_016884299.1:n.*1324del | |
| NM_000268.4:c.*1264del MANE Select | NP_000259.1:n.*1264del | |
| NM_181828.3:c.*1324del | NP_861966.1:n.*1324del | |
| NM_181829.3:c.*1324del | NP_861967.1:n.*1324del | |
| NM_181830.3:c.*1324del | NP_861968.1:n.*1324del | |
| NM_181832.3:c.*1339del | NP_861970.1:n.*1339del | |
| NR_156186.2:n.3534del | ||
| NM_181833.3:c.*1264del | NP_861971.1:n.*1264del |