gnomAD v2:
gnomAD v3:
gnomAD v4:
Joint Max Group AF
0.81762949 (AFR)
Genomes Max Group AF
0.81762949 (AFR)
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.111811603T>C , CM000669.2:g.111811603T>C | GRCh38 |
| NC_000007.13:g.111451659T>C , CM000669.1:g.111451659T>C | GRCh37 |
| NC_000007.12:g.111238895T>C | NCBI36 |
| NG_028060.1:g.399804A>G | |
| NG_028060.2:g.399809A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000428084.6:c.3006+271A>G (DOCK4) MANE Select | ENSP00000410746.1:n.3006+271A>G | |
| ENST00000437633.6:c.3006+271A>G (DOCK4) | ENSP00000404179.1:n.3006+271A>G | |
| ENST00000494651.7:c.2970+271A>G (DOCK4) | ENSP00000440944.3:n.2970+271A>G | |
| ENST00000423057.6:c.1361+271A>G (DOCK4) | ||
| ENST00000428084.5:c.3006+271A>G (DOCK4) | ENSP00000410746.1:n.3006+271A>G | |
| ENST00000437633.5:c.3006+271A>G (DOCK4) | ENSP00000404179.1:n.3006+271A>G | |
| ENST00000445943.5:c.3077+271A>G (DOCK4) | ||
| ENST00000469898.1:n.139+271A>G (DOCK4) | ||
| ENST00000494651.6:c.2970+271A>G (DOCK4) | ENSP00000440944.2:n.2970+271A>G | |
| NM_014705.3:c.3006+271A>G (DOCK4) | NP_055520.3:n.3006+271A>G | |
| NR_103806.1:n.109+2990T>C (DOCK4-AS1) | ||
| XM_006716188.1:c.3006+271A>G (DOCK4) | XP_006716251.1:n.3006+271A>G | |
| XM_006716189.1:c.3006+271A>G (DOCK4) | XP_006716252.1:n.3006+271A>G | |
| XM_011516716.1:c.3006+271A>G (DOCK4) | XP_011515018.1:n.3006+271A>G | |
| XM_011516717.1:c.3006+271A>G (DOCK4) | XP_011515019.1:n.3006+271A>G | |
| NM_001363540.1:c.3006+271A>G (DOCK4) | NP_001350469.1:n.3006+271A>G | |
| XM_006716189.2:c.3006+271A>G (DOCK4) | XP_006716252.1:n.3006+271A>G | |
| XM_017012819.1:c.3099+271A>G (DOCK4) | XP_016868308.1:n.3099+271A>G | |
| XM_017012820.1:c.3099+271A>G (DOCK4) | XP_016868309.1:n.3099+271A>G | |
| XM_017012821.1:c.3099+271A>G (DOCK4) | XP_016868310.1:n.3099+271A>G | |
| XM_017012822.1:c.3039+271A>G (DOCK4) | XP_016868311.1:n.3039+271A>G | |
| XM_017012823.1:c.3099+271A>G (DOCK4) | XP_016868312.1:n.3099+271A>G | |
| XM_017012824.1:c.3099+271A>G (DOCK4) | XP_016868313.1:n.3099+271A>G | |
| XM_017012825.1:c.3099+271A>G (DOCK4) | XP_016868314.1:n.3099+271A>G | |
| XM_024447006.1:c.2778+271A>G (DOCK4) | XP_024302774.1:n.2778+271A>G | |
| NM_014705.4:c.3006+271A>G (DOCK4) | NP_055520.3:n.3006+271A>G | |
| NM_001363540.2:c.3006+271A>G (DOCK4) MANE Select | NP_001350469.1:n.3006+271A>G |