Linked Data
dbSNP Id:
rs1441761381
gnomAD v2:
21-41149537-CTATT-C
gnomAD v3:
21-39777610-CTATT-C
gnomAD v4:
21-39777610-CTATT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.39777611_39777614del , CM000683.2:g.39777611_39777614del | GRCh38 |
| NC_000021.8:g.41149538_41149541del , CM000683.1:g.41149538_41149541del | GRCh37 |
| NC_000021.7:g.40071408_40071411del | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000380588.5:c.719-1479_719-1476del MANE Select | ENSP00000369962.4:n.719-1479_719-1476del | |
| ENST00000380588.4:c.719-1479_719-1476del | ENSP00000369962.4:n.719-1479_719-1476del | |
| ENST00000479378.1:n.825-1479_825-1476del | ||
| NM_001080444.1:c.719-1479_719-1476del | NP_001073913.1:n.719-1479_719-1476del | |
| XM_011529472.1:c.989-1479_989-1476del | XP_011527774.1:n.989-1479_989-1476del | |
| XM_011529473.1:c.989-1479_989-1476del | XP_011527775.1:n.989-1479_989-1476del | |
| XM_011529472.2:c.989-1479_989-1476del | XP_011527774.1:n.989-1479_989-1476del | |
| NM_001080444.2:c.719-1479_719-1476del MANE Select | NP_001073913.1:n.719-1479_719-1476del |