Linked Data
dbSNP Id:
rs2083747579
gnomAD v2:
21-46309143-CG-C
gnomAD v4:
21-44889228-CG-C
MyVariant Identifiers:
chr21:g.46309144del (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000021.9:g.44889232del , CM000683.2:g.44889232del | GRCh38 |
| NC_000021.8:g.46309147del , CM000683.1:g.46309147del | GRCh37 |
| NC_000021.7:g.45133575del | NCBI36 |
| NG_007270.2:g.44610del , LRG_76:g.44610del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000696946.1:n.1084+47del | ||
| ENST00000302347.10:c.1949+47del | ENSP00000303242.6:n.1949+47del | |
| ENST00000652462.1:c.1877+47del MANE Select | ENSP00000498780.1:n.1877+47del | |
| ENST00000302347.9:c.1877+47del | ENSP00000303242.5:n.1877+47del | |
| ENST00000355153.8:c.1877+47del | ENSP00000347279.4:n.1877+47del | |
| ENST00000397850.6:c.1877+47del | ENSP00000380948.2:n.1877+47del | |
| ENST00000397852.5:c.1877+47del | ENSP00000380950.1:n.1877+47del | |
| ENST00000397854.7:c.1706+47del | ENSP00000380952.3:n.1706+47del | |
| ENST00000397857.5:c.1877+47del | ENSP00000380955.1:n.1877+47del | |
| ENST00000475170.5:n.1277+47del | ||
| ENST00000498666.5:n.3933+47del | ||
| ENST00000523323.5:c.*1704+47del | ENSP00000427732.1:n.*1704+47del | |
| ENST00000610622.4:c.*568+47del | ENSP00000480700.1:n.*568+47del | |
| NM_000211.4:c.1877+47del | NP_000202.3:n.1877+47del | |
| NM_001127491.2:c.1877+47del | NP_001120963.2:n.1877+47del | |
| NM_001303238.1:c.1670+47del | NP_001290167.1:n.1670+47del | |
| XM_006724001.1:c.1670+47del | XP_006724064.1:n.1670+47del | |
| XM_006724001.2:c.1670+47del | XP_006724064.1:n.1670+47del | |
| NM_000211.5:c.1877+47del MANE Select | NP_000202.3:n.1877+47del | |
| NM_001127491.3:c.1877+47del | NP_001120963.2:n.1877+47del | |
| NM_001303238.2:c.1670+47del | NP_001290167.1:n.1670+47del |