Linked Data
dbSNP Id:
rs754349830
ExAC:
22:46748124 CT / C
gnomAD v2:
22-46748124-CT-C
gnomAD v4:
22-46352227-CT-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000022.11:g.46352228del , CM000684.2:g.46352228del | GRCh38 |
| NC_000022.10:g.46748125del , CM000684.1:g.46748125del | GRCh37 |
| NC_000022.9:g.45126789del | NCBI36 |
| NG_012173.1:g.21828del |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000465378.6:n.754-36del | ||
| ENST00000642923.1:c.601-36del | ENSP00000494255.1:n.601-36del | |
| ENST00000643137.1:c.601-36del | ENSP00000495331.1:n.601-36del | |
| ENST00000644006.1:c.*150-36del | ENSP00000493778.1:n.*150-36del | |
| ENST00000645026.1:n.757-36del | ||
| ENST00000645190.1:c.706-36del MANE Select | ENSP00000496496.1:n.706-36del | |
| ENST00000647301.1:c.*150-36del | ENSP00000496641.1:n.*150-36del | |
| ENST00000290846.8:c.706-36del | ENSP00000290846.4:n.706-36del | |
| ENST00000381019.3:c.706-36del | ENSP00000370407.3:n.706-36del | |
| ENST00000381021.7:c.*299-36del | ENSP00000370409.3:n.*299-36del | |
| ENST00000441818.5:c.*240-36del | ENSP00000393014.1:n.*240-36del | |
| ENST00000453630.5:c.*244-36del | ENSP00000398488.1:n.*244-36del | |
| ENST00000456595.5:c.*240-36del | ENSP00000413880.1:n.*240-36del | |
| ENST00000457572.5:c.*150-36del | ENSP00000407700.1:n.*150-36del | |
| ENST00000463785.1:n.174-36del | ||
| ENST00000479648.1:n.526-36del | ||
| ENST00000485175.5:n.666-36del | ||
| ENST00000486620.5:n.748-36del | ||
| NM_001282782.1:c.364-36del | NP_001269711.1:n.364-36del | |
| NM_001282783.1:c.286-36del | NP_001269712.1:n.286-36del | |
| NM_001282784.1:c.286-36del | NP_001269713.1:n.286-36del | |
| NM_001282785.1:c.706-36del | NP_001269714.1:n.706-36del | |
| NM_018006.4:c.706-36del | NP_060476.2:n.706-36del | |
| NR_104240.1:n.1015-36del | ||
| NR_104241.1:n.908-36del | ||
| XM_005261678.1:c.310-36del | XP_005261735.1:n.310-36del | |
| XM_005261681.1:c.310-36del | XP_005261738.1:n.310-36del | |
| XM_011530271.1:c.601-36del | XP_011528573.1:n.601-36del | |
| XM_011530272.1:c.706-36del | XP_011528574.1:n.706-36del | |
| XM_011530273.1:c.706-36del | XP_011528575.1:n.706-36del | |
| XM_011530274.1:c.364-36del | XP_011528576.1:n.364-36del | |
| XM_011530275.1:c.310-36del | XP_011528577.1:n.310-36del | |
| XM_011530271.2:c.601-36del | XP_011528573.1:n.601-36del | |
| XM_011530272.2:c.706-36del | XP_011528574.1:n.706-36del | |
| XM_011530273.2:c.706-36del | XP_011528575.1:n.706-36del | |
| XM_011530274.2:c.364-36del | XP_011528576.1:n.364-36del | |
| XM_024452260.1:c.601-36del | XP_024308028.1:n.601-36del | |
| XR_001755261.2:n.752-36del | ||
| XR_001755262.2:n.752-36del | ||
| NM_018006.5:c.706-36del MANE Select | NP_060476.2:n.706-36del | |
| NM_001282782.2:c.364-36del | NP_001269711.1:n.364-36del | |
| NM_001282783.2:c.286-36del | NP_001269712.1:n.286-36del | |
| NM_001282784.2:c.286-36del | NP_001269713.1:n.286-36del | |
| NM_001282785.2:c.706-36del | NP_001269714.1:n.706-36del | |
| NR_104240.2:n.702-36del | ||
| NR_104241.2:n.595-36del |