Linked Data
dbSNP Id:
rs1452240911
gnomAD v2:
1-12268585-TC-T
gnomAD v3:
1-12208528-TC-T
gnomAD v4:
1-12208528-TC-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.12208533del , CM000663.2:g.12208533del | GRCh38 |
| NC_000001.10:g.12268590del , CM000663.1:g.12268590del | GRCh37 |
| NC_000001.9:g.12191177del | NCBI36 |
| NG_029791.1:g.46531del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000376259.7:c.*1513del MANE Select | ENSP00000365435.3:n.*1513del | |
| ENST00000376259.6:c.*1513del | ENSP00000365435.3:n.*1513del | |
| ENST00000492361.1:n.2888del | ||
| NM_001066.2:c.*1513del | NP_001057.1:n.*1513del | |
| XM_011542060.1:c.*1513del | XP_011540362.1:n.*1513del | |
| XM_011542061.1:c.*1513del | XP_011540363.1:n.*1513del | |
| XM_011542062.1:c.2947del | XP_011540364.1:n.2947del | |
| XM_011542063.1:c.*1513del | XP_011540365.1:n.*1513del | |
| XM_011542060.2:c.*1513del | XP_011540362.1:n.*1513del | |
| XM_011542063.2:c.*1513del | XP_011540365.1:n.*1513del | |
| XM_017002214.1:c.*1513del | XP_016857703.1:n.*1513del | |
| XM_017002215.1:c.*1513del | XP_016857704.1:n.*1513del | |
| NM_001066.3:c.*1513del MANE Select | NP_001057.1:n.*1513del |